USRE31343E - Piperidine derivatives - Google Patents

Piperidine derivatives Download PDF

Info

Publication number
USRE31343E
USRE31343E US05/938,849 US93884978A USRE31343E US RE31343 E USRE31343 E US RE31343E US 93884978 A US93884978 A US 93884978A US RE31343 E USRE31343 E US RE31343E
Authority
US
United States
Prior art keywords
sub
carbon atoms
residue
iadd
iaddend
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US05/938,849
Inventor
Brian Holt
Donald R. Randell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis Corp
Original Assignee
Ciba Geigy Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ciba Geigy Corp filed Critical Ciba Geigy Corp
Application granted granted Critical
Publication of USRE31343E publication Critical patent/USRE31343E/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
    • C08K5/3432—Six-membered rings
    • C08K5/3435—Piperidines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/40—Oxygen atoms
    • C07D211/44—Oxygen atoms attached in position 4
    • C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02—Boron compounds
    • C07F5/04—Esters of boric acids
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
    • C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
    • C09K15/30—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing heterocyclic ring with at least one nitrogen atom as ring member

Definitions

  • the present invention relates to new piperidine derivatives, and in particular to new piperidine derivatives substituted at the 1- and 4- positions and having value as stabilisers for polymeric materials.
  • acyl group derived from an aliphatic, alicyclic or heterocyclic mono-carboxylic acid an N-substituted carbamoyl group derived from an N-substituted carbamic acid, an N-substituted thiocarbamoyl group derived from an N-substituted thiocarbamic acid, a monovalent group obtained by removing an hydroxyl group from an oxo-acid, an alkyl group, a cycloalkyl group, an aralkyl group, an aryl group or a group having the formula: ##STR3## wherein R 1 ' and R 2 ' have their previous significance; when n' is 2, R 2 is a diacyl group derived from an aliphatic, alicyclic, aromatic or heterocyclic dicarboxylic acid, a dicarbamoyl group derived from a dicarbamic acid, a bis-thiocarbamoyl group
  • .Iadd.R 3 '.Iaddend. is a triacyl group, derived from an aliphatic, alicyclic, aromatic or heterocyclic tricarboxylic acid, a tricarbamoyl group derived from tricarbamic acid, a tris-thiocarbamoyl group derived from a tris-thiocarbamic acid, a trivalent group obtained by removing three hydroxyl groups from an oxo-acid, an alkanetriyl group, arenetriyl group or an arenetriyl trialkylene group.
  • n 1, 2, 3 or 4
  • R 1 is a monovalent residue and is an alkyl residue having from 1 to 20, preferably 1 to 12 carbon atoms, an alkenyl or alkynyl residue having from 3 to 20, preferably 3 to 12 carbon atoms, an aralkyl residue having from 7 to 12 carbon atoms, or a residue having the formula: ##STR5## wherein m is 1, 2 or 3; R 4 is hydrogen, methyl or phenyl residue, X 2 is halogen, cyano, ##STR6## --COR 5 , --CO.OR 5 , --CO.SR 5 , or --CONR 5 R 6 and X 1 is hydroxyl, halogen, cyano, --OR 5 , ##STR7## wherein R 5 is an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 2 to 20 carbon atoms, a residue having the formula: ##STR5## wherein m is 1, 2 or 3; R 4 is hydrogen,
  • R 3 is a divalent residue and is an alkylene residue having from 1 to 20 carbon atoms, an alkenylene residue having from 2 to 20, preferably 3 to 20, carbon atoms, an alkynylene residue having from 2 to 20, preferably 3 to 20, carbon atoms, cycloalkylidene residue having from 5 to 12 carbon atoms, an arylene residue having 6 to 14 carbon atoms, an aralkylene residue having from 8 to 14 carbon atoms or an aliphatic, aromatic or heterocyclic diacyl residue, ##STR11## an aliphatic or aromatic dicarbamoyl or dithiocarbamoyl residue, sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or a boric acid.
  • R 3 is a trivalent residue and is an .[.arenetriyl.]. .Iadd.alkanetriyl .Iaddend.or an arenetriyl-trialkylene residue, an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric, o-phosphorous or o-boric acid; and
  • R 3 is a tetravalent residue and is an alkane tetrayl residue, or a tetraacyl residue derived from an aliphatic or aromatic tetracarboxylic acid or from o-silicic acid;
  • R 1 and/or R 3 may be an alkyl residue having from 1 to 20 carbon atoms, preferred 1 to 18, examples of this substituent are methyl, ethyl, n-propyl, n-butyl, sec-butyl, t-butyl, n-hexyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-hexadecyl or n-octadecyl residue and eicosyl.
  • alkyl substitutents R 1 and/or R 3 having from 5 to 20, especially 5 to 12 carbon atoms are preferred.
  • a sub-group of alkyl residues R 1 is that containing from 1 to 4 carbon atoms, preferably methyl.
  • R 1 and/or R 3 is an alkenyl residue having from 3 to 20 carbon atoms
  • substituents are allyl, methallyl, 3-hexenyl, 4-octenyl, 6-decenyl, 10-undecenyl, and8-octadecenyl residues, however the preferred substituents in this group are allyl and methallyl residues.
  • R 1 and/or R 3 are alkynyl they may be for example propargyl, but-1- and -2-ynyl, pent-1-ynyl, hex-1-ynyl, oct-1-ynyl, dec-1-ynyl, dodec-1-ynyl, tetradec-1-ynyl and octadec-1-ynyl.
  • the preferred alkynyl substituents however are propargyl and methylpropargyl.
  • R 1 and/or R 3 is an aralkyl residue
  • suitable examples are benzyl, ⁇ -phenethyl, ⁇ -methylbenzyl, ⁇ -dimethylbenzyl, ⁇ -naphthylmethyl and p-methyl- ⁇ -methylbenzyl residues.
  • Benzyl is preferred.
  • R 1 and/or R 3 substituents is substituted alkyl derivatives having the formula: ##STR12## wherein m, R 4 , X 1 and X 2 have their previous significance, but wherein, however, R 4 is preferably hydrogen and m is preferably 1.
  • examples of this substituents R 1 and/or R 3 are 2-hydroxyethyl, 2- and 3-hydroxypropyl, 3- and 4-hydroxybutyl, 4-hydroxypentyl and 2-hydroxy-2-phenyl ethyl, preferably 2-hydroxyethyl, 2-hydroxypropyl and 2-hydroxy-2-phenylethyl.
  • R 1 and/or R 3 include 2-chloro- and 2-bromo ethyl, 2- and 3-chloro- and 2- and 3-bromopropyl, 3- and [4-chorobutyl and 2-chloro-2-phenyl ethyl, preferably 2-choroethyl, 2-chloropropyl and 2-chloro-2-phenylethyl.
  • R 1 and/or R 3 include cyanomethyl, 1- and 2- cyanobutyl, 4-cyanopentyl, 2-cyano-2-phenylethyl groups, preferably a 2-cyanoethyl group.
  • R 1 and/or R 3 may be 2,3-epoxy-n-propyl, 2,3 -epoxy-methylpropyl, but the preferred epoxyalkyl substituent is 2,3 -epoxy-n-propyl.
  • X 1 is --OR 5 , --OCOR 5 , --OCSR 5 , --OCONR 6 R 5 , --CSNR 6 R 5 , or when X 1 and/or X 2 are --COR 5 , --COOR 5 , --COSR 5 , --CONR 6 R 5 and the group R 5 is alkyl, then the alkyl group preferably has from 1 to 12, most preferred 1 to 2, carbon atoms; when R 5 is an alkenyl residue, then it preferably contains 2 to 4 carbons; when R 5 is a cycloalkyl group it preferably contains 6 carbon atoms; when R 5 is an aryl residue it preferably contains 6 or 7 carbons; and when R 5 is an aralykyl residue, it preferably has 7 or 8 carbon atoms.
  • R 5 and R 6 together with the nitrogen atom to which they are bound can form a 5- or 6-membered ring such as the pyrrolidinyl-, imidazolidinyl-, pyrazolidinyl-, piperidinyl-, piperazinyl- or morpholinyl ring.
  • R 1 and/or R 3 within this sub-group ae 2-methoxyethyl, 2-ethoxyethyl, 2-propoxyethyl, 2-butoxyethyl, 2-methoxypropyl, 2- and 3-ethoxypropyl, 2- and 3-n-butoxypropyl, 3- and 4-methoxybutyl, 3- and 4-ethoxybutyl, 3- and 4-butoxybutyl, 4-methoxypentyl, 4-ethoxypentyl, 4-n-butoxypentyl, 2-methoxy-2-phenyl ethyl, 2-ethoxy-2-phenyl ethyl; 2-acetoxyethyl, 2-n-propionoxyethyl, 2-benzoyloxy ethyl, 2-acetoxypropyl, 2-n-propionoxypropyl, 4-acetoxybutyl, 4-n-propionoxybutyl, 4-acetoxypentyl, 4-n-propionoxypentyl, 4-
  • R 7 is an unsubstituted aliphatic or substituted aliphatic residue having from 1 to 20, preferably 1 to 19, carbon atoms
  • R 7 may be a methyl, ethyl, propyl, butyl, hexyl, n-octyl, 2-ethylhexyl, n-decyl, n-undecyl, n-tridecyl, n-tetradecyl, n-hexadecyl, n-heptadecyl and eicosyl, chloroethyl, chlorohexyl, methylthioethyl, ethylthioethyl, octylthioethyl, or dodecylthioethyl residue; alkenyl residues R 7 have from 2 to 20, preferably 2 to 17, most
  • acyl groups R 1 and/or R 3 are formyl, acetyl, propionyl, n-butyryl, hexanoyl, heptanoyl, octanoyl, 2-ethylhexanoyl, 2,2,4-trimethylpentanoyl, n-decanoyl, n-dodecanoyl, n-tetradecanoyl, n-hexadecanoyl, n-octadecanoyl, n-eicosoyl, acryloyl, ⁇ -methacrylol, crotonoyl, undec-10-enoyl, octadec-9-enoyl, ⁇ -methylthiopropionyl, methylthioacetyl, ⁇ -octylthiopropionyl, ⁇ -dodecylthiopropionyl, cyclopentano
  • R 1 and/or R 3 may also be a carbamoyl or thiocarbamoyl residue having the formula: ##STR13## wherein X 3 is --O-- or --S--, R 8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms and R 9 is hydrogen, an alkyl residue having from 1 to 20, preferably 1 to 8, carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an unsubstituted .[.alkyl.].
  • aryl for instance, alkyl or halogen-substituted aryl residue having from 6 to 12, preferably 6 to 10, carbon atoms.
  • suitable residues within this group are carbamoyl, N-methylcarbamoyl, N-ethyl-carbamoyl, N-n-propylcarbamoyl, N-isopropylcarbamoyl, N-n-butylcarbamoyl, N-n-pentylcarbamoyl, N-n-octylcarbamoyl, N-n-decylcarbamoyl, N-n-dodecylcarbamoyl, N-n-octadecyl, N-n-eisocylcarbamoyl, N-allylcarbamoyl, N-methallylcarbamoyl, N-
  • R 2 is an alkyl residue it is for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, preferably methyl, as alkenyl residue
  • R 2 is for example allyl, methallyl, 3-hexenyl, 4-octenyl, 6-decenyl, 10-undecenyl or 8-octadecenyl, peferably allyl or methallyl and as alkynyl residue for example propargyl, but-1- and -2-ynyl, penta-1-ynyl, hex-1-ynyl, oct-1-ynyl, dec-1-ynyl, dodec-1-ynyl, tetradec-1-ynyl and octadec-1-ynyl, preferably propargyl
  • R 2 as cycloalkyl is
  • R 3 may be the same as R 1 . If R 3 is alkyl it is preferably an alkyl group having from 3 to 18 carbon atoms.
  • R 3 represents an aryl residue it is for example an aromatic residue having 6 to 20 carbon atoms, preferably an aryl residue having 6 to 12 carbon atoms, most preferred phenyl.
  • R 3 is, for example an alkylene residue having from 1 to 20, preferably 2 to 6, carbon atoms such as methylene, ethylene, trimethylene, tetramethylene or hexamethylene residue.
  • Alkenylene residues R 3 preferably contain 3 to 20, most preferred 3 or 4 carbons, and may be, for instance a 1,3-propen-ene or 1,4-buten-2-ene residue.
  • Alkynylene residues R 3 preferably contain 3 to 20, most preferred 4 carbon atoms and may be, for instance a 1:4 but-2-ynylene residue.
  • R 3 is a cycloalkylidene residue, it preferably contains 7 or 8 carbon atoms, for instance a cyclohexyldimethylene residue.
  • R 3 is arylene it has preferably 6 to 12 carbon atoms and it may be for example 1,3-phenylene, or 4,4'-diphenylene.
  • R 3 is aralkylene it may be for example ⁇ , ⁇ -p-xylylene.
  • Diacyl residues R 3 include those derived from an aliphatic, aromatic or heterocyclic dicarboxylic acid.
  • aliphatic dicarboxylic acids are those having from 2 to 20, preferably alkan dicarboxylic acids having 6 to 10 carbon atoms such as malonic, succinic, glutaric, adipic, pimelic, suberic, azelaic, sebacic, 1,12-dodecanedioic, 1,18 -octadecanedioic, 1,20-docosanedioic acid and N-methyliminodiacetic acid.
  • aromatic diacyl residues are those derived from phthalic, isophthalic and terephthalic acids, each optionally ring-substituted, for instance by halogen, an alkyl or alkoxy group each having from 1 to 20 carbon atoms, a hydroxy or tertiary amino group.
  • heterocyclic dicarboxylic acids examples include 2,5-thiophene dicarboxylic acid or 2,5-furandicarboxylic acid.
  • R 3 is for example an aliphatic or aromatic dicarbamoyl residue such as a divalent .[.alkyl.]. .Iadd.alkylene .Iaddend.dicarbamoyl residue for example the divalent residue of butan-1,4-dicarbamoyl or hexan-1,6-dicarbamoyl or such as a divalent .[.aryl.]. .Iadd.arylene .Iaddend.dicarbamoyl residue such as the divalent residue of .[.phenyl.]. .Iadd.phenylene.Iaddend.-1,4-dicarbamoyl.
  • R 3 is for example an aliphatic or aromatic dithicarbamoyl residue such as a divalent .[.alkyl.]. .Iadd.alkylene .Iaddend.dithicarbamoyl residue for example the divalent residue of butan-1,4-dithiocarbamoyl or hexan-1,6-dithiocarbamoyl or such as an divalent .[.aryl.]. .Iadd.arylene .Iaddend.dithiocarbamoyl residue sue as the divalent residue of .[.phenyl.]. .Iadd.phenylene.Iaddend.-1,4-dithiocarbamoyl.
  • R 3 is, for instance, a triacyl group derived from an aliphatic tricarboxylic acid such as nitrilotriacetic acid, tricarballylic acid, from an aromatic tricarboxylic acid such as benzene tricarboxylic acid or from an inorganic acid such as o-phosphorous, o-phosphoric or o-boric acid, or oxyacids, for example, benzene-1,3,5-trisulphonic acid.
  • an aliphatic tricarboxylic acid such as nitrilotriacetic acid, tricarballylic acid
  • an aromatic tricarboxylic acid such as benzene tricarboxylic acid
  • an inorganic acid such as o-phosphorous, o-phosphoric or o-boric acid, or oxyacids, for example, benzene-1,3,5-trisulphonic acid.
  • R 3 is, for instance, a tetracyl group derived from a tetracarboxylic acid, such as ethylene diamine, tetracarboxylic acid, from the tetracarboxylic acids described in British Patent Specification No. 1080335, 1,2,4,5,-benzene tetracarboxylic acid or from o-silicic acid.
  • a tetracyl group derived from a tetracarboxylic acid such as ethylene diamine, tetracarboxylic acid, from the tetracarboxylic acids described in British Patent Specification No. 1080335, 1,2,4,5,-benzene tetracarboxylic acid or from o-silicic acid.
  • R 3 preferably represents an acyl or an N- substituted carbamoyl, an alkylene group, a substituted alkylene or an aralkyl group.
  • R 1 preferably represents an alkyl, alkenyl, or substituted alkyl group such as hydroxyalkyl, alkylcarbonyloxy or aralkyl group.
  • Examples of compounds of the present invention are:
  • Toluene-2 4 ⁇ -bis[4-carbamoyloxy-1-(2'-hydrocyethyl)-2,2,6,6-tetramethylpiperidine].[.Diphenylmethane.].-4',4"-bis.Iadd.Diphenylmethane-[4-carbamoyloxy-1-(2'-cyanoethyl)-2,2,6,6-tetramethylpiperidine]
  • the invention also includes salts of the compounds of Formula I, for instance salts of inorganic acids such as phosphates, carbonates, sulphates and chlorides and salts of organic acids such as acetates, stearates, maleates, citrates, tartrates, oxalates, benzoates and substituted carbamic acids.
  • inorganic acids such as phosphates, carbonates, sulphates and chlorides
  • organic acids such as acetates, stearates, maleates, citrates, tartrates, oxalates, benzoates and substituted carbamic acids.
  • R 1 or R 3 can be represented by a monovalent, divalent or trivalent group obtained by removing 1 to 3 hydroxyl groups from a sulphonic acid, a sulphinic acid, a disulphonic acid, a phosphorus containing acid, such as o-phosphoric or o-phosphorous acid or a boric acid.
  • the following list shows compounds with acid radicals for R 3 .
  • the same radicals are also examples for R 1 .
  • a preferred sub-group of compounds of formula 1 are those compounds having the formula: ##STR14## and their salts, wherein Y is an alkyl group having from 1 to 20, preferably 1 to 4, carbon atoms, alkenyl having from 3 to 20 carbon atoms or an aralkyl residue, preferably having from 7 to 9 carbon atoms, and n 1 is 1 or 2; when n 1 is 1, R is hydrogen or a monovalent aliphatic residue having from 1 to 20, preferably 6 to 20 carbon atoms, a monovalent alicyclic residue having from 5 to 12 carbon atoms, or a monovalent aromatic residue having from 6 to 20 carbon atoms; or ##STR15## and when n 1 is 2, R is a divalent aliphatic residue having from 1 to 20, preferably 4 to 20 carbon atoms, a divalent alicyclic residue having from 5 to 12 carbon atoms or a divalent aromatic residue having from 6 to 14 carbon atoms.
  • Two sub-groups of the compounds of the formula Ia
  • substituents Y are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.butyl, n-hexyl, n-octyl, n-dodecyl, n-octadecyl, eicosyl, allyl, methallyl, oleyl, benzyl, ⁇ -methylbenzyl, p-methylbenzyl and p-methyl- ⁇ -methylbenzyl, However, it is particularly preferred that Y is methyl.
  • R can be hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.butyl, t-butyl, n-pentyl, 1-ethylpropyl, 2-methylbutyl, n-hexyl, 2-methylpentyl, n-heptyl, 2-ethylpentyl, n-octyl, 2,2,4-trimethylpentyl, n-decl, n-undecyl, n-tridecyl, n-pentadecyl, n-heptadecyl, eicosyl, vinyl ⁇ - or ⁇ -methylvinyl, dec-9-enyl, heptadec-8-enyl, ⁇ -methythioethyl, ⁇ -octylthioethyl, ⁇ -dodecylthioe
  • R are those listed above containing from 6 to 20 carbon atoms, as well as the group having the formula: ##STR17## wherein R 10 and R 11 are the same or different and each is an alkyl group having from 1 to 6, preferably 1 to 4 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, sec.butyl, t-butyl, t-pentyl, (1,1,-dimethylpropyl), t-hexyl (1,1,-dimethylbutyl), but preferably methyl, isopropyl or t-butyl groups: A is -CH 2- , ##STR18## and p is 0 or 1.
  • R can be methylene, 1,2,-ethylene, 1,4-n-butylene, 1,8-n-octylene, 2,2,4-trimethyl-1, 4-butylene, 1,10-n-decylene, 1,2-eicosylene, vinylene, propenylene, 1,2-, 1,3- and 1,4-cyclohexylene, cyclohexyl-3-ene, 11,2-, 1,3- and 1,4-phenylene, p-xylylene, 1,4-, and 1,5-naphthylene, diphenylene or diphenylmethylene.
  • a further preferred sub-group of compounds of formula I are those having the formula: ##STR19## and is salts wherein Y 1 is an alkyl residue having from 1 to 12 carbon atoms, an alkenyl residue having from 3 to 12 carbon atoms or an aralkyl residue having from 7 to 9 carbon atoms and R 12 is hydrogen or an alkyl or alkylen containing up to 20 carbon atoms, and substituted alkyl having the formula ##STR20## wherein m is 1, 2 or 3, R 4 is hydrogen or methyl, .[.S 1 .].
  • X 1 is halogen or methoxy and X 2 is halogen or R 12 is an alkenyl or alkenylen having up to .Badd.20 carbon atoms, a cycloalkyl or cycloalkyliden having 5 to 12 carbon atoms, an aryl or arylen having 6 to 12 carbon atoms and q is 1 or 2.
  • Two sub-groups of compounds of the formula Ib are those having as Y 1 alkyl from 1 to 4 and alkyl having 5 to 12 carbom atoms.
  • R 12 can be for example hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, secbutyl, t-butyl, n-pentyl, 2-ethylpropyl, 2-methylbutyl, n-hexyl, 2-methylpentyl, n-heptyl, 2-ethylpentyl, n-octyl, 2-ethylhexyl, 2,2,4-trimethylpentyl, n-decyl, n-dodecyl, n-tetradecyl, n-octadecyl, eicosyl, mesityl, allyl, oleyl, cyclopentyl, cyclohexyl, methylcyclohexyl, t-butylcyclohexyl, t-octylcylohexyl, eicosyl
  • Preferred monovalent groups R 12 are hydrocarbyl groups such as methyl, ethyl, propyl, isopropyl, n-butyl, 2-ethylhexyl, dodecyl, octadecyl, allyl, oleyl, cyclohexyl, benzyl, phenyl, o-, m- and p-tolyl, 2,4- and 2,6-xylyl and naphthyl.
  • R 12 can be for example methylene, 1,2-ethylene, 1,4-n-butylene, 1,6-n-hexylene, 1,8-n-octylene, 2,4,4-trimethyl-1,6-hexylene, 1,10-n-decylene, 1,2-eicosylene, 1,2-eicosenylene, 1,3- and 1,4-cyclohexylene, 1,3- and 1,4-phenylene, 2,4-tolylene, 1,5-naphthylene, 4,4'-diphenylene, 4'-diphenylemethylene, 3,3'-dimethyl-4,4'-diphenylene, 3,3'-dimethyl-4,4'-diphenylmethylene.
  • Preferred divalent groups R 12 are 1,2-ethylene, 1,6-hexylene, 2,4,4-trimethyl-1,6-hexylene, 1,3- and 1,4-phenylene, 2,4-tolylene, 1,5-naphthylene, 4,4'-diphenylmethylene.
  • examples of the group Y 1 are methyl, ethyl, n-propyl, isopropyl, n-butyl, secbutyl, n-hexyl, n-octyl, n-dodecyl, allyl, ⁇ -methallyl, 10-undecenyl, benzyl, ⁇ -methylbenzyl, p-methylbenzyl, p-methyl- ⁇ -methylbenzyl, ⁇ -naphthylmethyl.
  • Particularly preferred are straight or branched alkyl having 1 to 4 carbon atoms and for reasons of ease of preparation the most preferred meaning for Y 1 is methyl.
  • R 3 is a monovalent residue and is an alkyl residue having from 1 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an alkenyl or alkynyl residue having from 3 to 20 carbom atoms, an aralkyl residue having from 7 to 12 carbon atoms, or a residue having the formula: ##STR21## wherein m is 1, 2 or 3, R 4 is a hydrogen, methyl or phenyl residue, X 2 is halogen, cyano, ##STR22## --COR 5 , --CO.OR 5 , --CO.SR 5 or --CONR 5 R 6 and X 1 is hydroxyl, halogen, cyano, -OR 5 , ##STR23## wherein R 5 is an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 2 to 20 carbon atoms, a cycloalkyl residue having 5
  • R 3 is an acyl group ##STR25## wherein R 7 is hydrogen, an unsubstituted aliphatic or substituted aliphatic residue having from 1 to 20 carbon atoms, an alkenyl or alkynyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, an aromatic residue having from 6 to 20 carbon atoms, or an heterocyclic residue, or R 3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid, when n is 2,R 3 is an divalent residue of an aliphatic, aromatic or heterocyclic diacyl, the group --CO-- or --CO.CO--, a sulphinyl or sulphonyl residue or
  • R 3 is a carbamoyl residue having the formula: ##STR26## wherein R 8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, and R 9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an unsubstituted aryl or substituted aryl residue having from 6 to 12 carbon atoms; and when n is 2 R 3 is a divalent aliphatic or aromatic dicarbamoyl residue.
  • R 3 is a thiocarbamoyl residue having the formula: ##STR27## wherein R 8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, and R 9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an unsubstituted aryl or substituted aryl residue having from 6 to 12 carbon atoms; and when n is 2,R 3 is a divalent aliphatic or aromatic dithiocarbamoyl.
  • R 3 is a monovalent residue and is an alkyl residue having from 1 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an alkenyl or alkynyl residue having from 3 to 20 carbon atoms, an aralkyl residue having from 7 to 9 carbon atoms, or a residue having the formula: ##STR28## wherein m is 1, 2 or 3, R 4 is a hydrogen, methyl or phenyl residue, X 2 is halogen, cyano, ##STR29## --COR 5 , --CO.OR 5 , --CO.SR 5 or --CONR 5 R 6 and X 1 is hydroxyl, halogen, cyano, --OR 5 , --O--CO.R 5 , --OCSR 5 , --O.CO.NR 5 R 6 ,--CO.R 5 , --CO.OR 5 , --CO.SR 5 , --CO.NR 5
  • R 3 is an acyl group ##STR31## wherein R 7 is an aliphatic or substituted aliphatic residue having from 1 to 20 carbon atoms, an alkenyl or alkynyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, an aromatic residue having from 6 to 12 carbon atoms or an heterocyclic residue, with the proviso that only one of R 1 and R 3 can represent an unsaturated acyl group or R 3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid, when n is 2, R 3 is a divalent residue of an aliphatic, aromatic or heterocyclic diacyl residue, a carbonyl, sulphinyl or s
  • R 8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms
  • R 9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an aryl or substituted aryl residue having from 6 to 12 carbon atoms
  • R 3 is a divalent residue of an aliphatic or aromatic dicarbamoyl residue..
  • R 8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms
  • R 9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an aryl or substituted aryl residue having from 6 to 12 carbon atoms
  • R 3 is a divalent residue of an aliphatic or aromatic dithiocarbamoyl residue..
  • R 5 is alkyl having .Badd.1 or 2carbon atoms or phenyl or R 1 is a group of the formula and R 2 is hydrogen and R 3 when n is 1 is alkyl having 3 to 18 carbon atoms, alkenyl having 3 carbon atoms, propargyl, benzyl, .[.--CH 2 CH 2 CH.]. .Iadd.CH 2 CH 2 CN .Iaddend.or a group of the formula
  • X 2 is ##STR37## .[.of.]. .Iadd.or is a group .Iaddend.of the formula ##STR38## wherein R 7 is alkyl having 1 to 19 carbon atoms, CH 3 (CH 2 ) 11 --S--CH 2 --, cycloalkyl having 6 to 10 carbon atoms, alkenyl having 2 to 17 carbon atoms, unsubstituted aralkyl having 7 to 13 carbon atoms, C 6 H 5 -CH ⁇ CH--, aralkyl substituted by hydroxy or butyl, unsubstituted aryl having 6 to 10 carbon atoms, aryl substituted by alkyl having 1 to 4 carbon atoms, CH 3 O--, Cl, OH or ##STR39## or of the formula ##STR40## wherein R 9 is alkyl having 1 to 8carbon atoms, alkenyl having 3 carbon atoms, cyclohexyl, unsubstituted ary
  • R 3 is an acyl group ##STR44## wherein R 7 is hydrogen, an substituted aliphatic residue having from 1 to 20 carbon atoms, a alkenyl or alkynyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, or an heterocyclic residue, or R 3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid, or when n is 2, R 3 is an divalent residue of heterocyclic diacyl residue or a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a
  • R 3 is an acyl group ##STR45## wherein R 7 is hydrogen, a cycloliphatic residue having from 5 to 12 carbon atoms or a heterocyclic residue or R 3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid or when n is 2, R 3 is a divalent residue of a heterocyclic diacyl or a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or when n is 4, R 3 is a tetraacyl residue derived from an aliphatic tetracarboxylic acid.
  • R 7 is hydrogen, substituted aliphatic residue having from 1 to 20 carbon atoms, an alkenyl or alkylnyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, or an heterocyclic residue
  • R 3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid or when n is 2
  • R 3 is a divalent residue of heterocyclic diacyl residue or a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phospho
  • R 7 is hydrogen, a cycloaliphatic residue having from 5 to 12 carbon atoms or a heterocyclic residue or R 3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid or when n is 2, R 3 is a divalent residue of a heterocyclic diacyl or a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or when n is 4, R 3 is a tetraacyl residue derived from an aliphatic tetracarboxylic acid..].
  • R 3 is an acyl group ##STR48## wherein R 7 is an unsubstituted aliphatic residue having from 1 to 20 carbon atoms or an aromatic residue having from 6 to 20 carbon atoms and when n is 2, R 3 is an divalent aliphatic or aromatic diacyl residue or the groups --CO-- or --COCO-- and when n is 3, R 3 is a trivalent residue and is an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric, o-phosphorous or o-boric acid and when n is 4, R 3 is a tetravalent residue of a tetraacyl residue derived from an aromatic tetracarboxylic acid or from o-silicic acid.
  • R 7 is an unsbustituted aliphatic residue having from 1 to 20 carbon atoms or an aromatic residue having from 6 to 12 carbon atoms and when n is 2, R 3 is an divalent aliphatic or aromatic diacyl residue or the carbonyl group and when n is 3, R 3 is a trivalent residue and is an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric o-phosphorous or o-boric acid and when n is 4, R 3 is a tetravalent residue of a tetraacyl residue derived from an aromatic tetracarboxylic acid or from o-silicic acid..].
  • R is a monovalent aliphatic residue having from 1 to 20 carbon atoms or a monovalent aromatic residue having from 6 to 20 carbon atoms and when n is 2, R is a divalent aliphatic residue having from 1 to 20 carbon atoms or a divalent aromatic residue having from 6 to 20 carbon atoms.
  • n 1, 2, 3 or 4
  • R 1 is a monovalent residue and is an alkyl residue having from 1 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an alkenyl or alkynyl residue having from 3 to 20 carbon atoms, an aralkyl residue having from 7 to 9 carbon atoms, or a residue having the formula: ##STR51## wherein m is 1, 2 or 3, R 4 is a hydrogen, methyl or phenyl residue, X 2 is halogen, cyano, ##STR52## --COR 5 , --CO.OR 5 , --CO.SR 5 , --CONR 5 R 6 or CS.NR 5 R 6 and X 1 is hydroxyl, halogen, cyano, ##STR53## --OR 5 , --O--CO.R 5 , OCSR 5 , --O.CO.
  • R 2 is an alkyl residue having from 1 to 4 carbon atoms, an alkenyl or alkynyl residue having 3 to 20, carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an aryl residue having from 6 to 11 carbon atoms or an aralkyl residue having from 7 to 9 carbon atoms or also hydrogen; and when n is 1, R 2 is a monovalent radical having the same significance as R 1 , with the proviso that only one of R 1 and R 3 can represent a unsaturated acyl group or R 3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid, or R 3 is an aryl residue or a residue having the formula: ##STR54## wherein R 1 ' is hydrogen or R 1 ' has the same significance as R 1 .
  • R 3 is a divalent residue and is an alkylene residue having from 1 to 20 carbon atoms, an alkenylene residue having from 3 to 20 carbon atoms, an alkynylene residue having from 3 to 20 carbon atoms, an arylene residue having 6 to 14 carbon atoms, an aralkylene residue having from 8 to 14 carbon atoms or an aliphatic, aromatic or heterocyclic diacyl residue, an aliphatic or aromatic dicarbamoyl or dithiocarbamoyl, a carbonyl, sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or a boric acid; when n is 3, R 3 is a trivalent residue or an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric, o-phosphorous or o-boric acid or an alkanetriyl,
  • R' and R" are the same or different and each is a straight or branched alkyl group, having from 1 to 4 carbon atoms, or R' and R" together with the carbon atom to which they are attached form a cycloalkyl residue having from 5 to 12 carbon atoms;
  • Y is an alkyl group having from 1 to 20 carbon atoms, preferably 1 to 4, carbon atoms, alkenyl having from 2 to 20 carbon atoms or an aralkyl residue having from 7 to 9 carbon atoms and n 1 is 1 or 2; when n is 1, R is hydrogen or a monovalent aliphatic residue having from 1 to 20, preferably 6 to 20 carbon atoms, a monovalent alicyclic residue having from 5 to 12 carbon atoms, or a monovalent aromatic residue having from 6 to 20 carbon atoms; and when
  • n 1 and R is a monvalent aliphatic, alicyclic or aromatic residue having from 6 to 20 carbon atoms and this group has the formula: ##STR56## wherein R 10 and R 11 are the same or different and each is an alkyl group having from 1 to 6 carbon atoms, A is ##STR57## or --CH 2 CH 2 -- and p is 0 1, or
  • n 2 and R is a methylene, 1,2-ethylene, 1,4-butylene, 1,8-n-octylene, 2,2,4-trimethyl-1, 4-butylene, 1,10-n-decylene, 1,2-eicosylene, vinylene, propenylene, 1,2-, 1,3- or 1,4-cyclohexylene, cyclohexyl-3-ene, 1,2-, 1,3- or 1,4-phenylene, p-xylylene, 1,4- or 1,5-naphthylene, diphenylene or diphenylmethylene residue or the group --CH 2 CH 2 S CH 2 CH 2 -- or R is absent.
  • the following compounds of the formula IV are also compounds of the present invention: ##STR58## and its salts wherein R III and R IV are the same or different and each is a straight- or branched alkyl residue having from 1 to 12 carbon atoms or R III and R IV together with the carbon atom to which they are each attached form a cycloalkyl group having from 5 to 12 carbon atoms, Y is a straight- or branched alkyl residue having from 1 to 12 carbon atoms, an alkenyl residue having from 3 to 12 carbon atoms or an aralkyl residue having from 7 to 12 carbon atoms and R 12 is hydrogen or a saturated or unsaturated hydrocarbyl residue containing up to 20 carbon atoms optionally substituted, .[.Y.]. .Iadd.by .Iaddend.halogen or alkoxy having from 1 to 4 carbon atoms and q is 1 or 2.
  • Sub-groups of the compounds of formula IV are:
  • R 12 is a methyl, ethyl, propyl, isopropyl, n-butyl, 2-ethylhexyl, dodecyl, octadecyl, allyl, oleyl cyclohexyl, benzyl, phenyl o-, m- or p-tolyl, 2,4- or 2,6-xylyl or a naphthyl residue.
  • R 12 is a 1,2-ethylene, 1,6-hexylene, 2,4,4-trimethyl-1,6-hexylene, 1,3- or 1,4-phenylene, 2,4-tolylene, 1,5-naphthylene or 4,4'-diphenylmethylene residue.
  • a first process in which a compound of formula I is produced comprising reacting, in the presence of an acidbinding agent, a piperidinol having the formula: ##STR59## wherein R 1 and R 2 have their previous significance, with an acid halide having the formula:
  • R 3 and n have their previous significance and hal represents a halogen atom, preferably a chlorine atom.
  • Suitable acid binding agents are organic bases such as triethylamine; alternatively, an excess amount of the amine V can serve as the acid binding agent.
  • reaction is conveniently carried out by heating the reactants together in a solvent such as cyclohexane, benzene or toluene which is inert under the reaction conditions.
  • a solvent such as cyclohexane, benzene or toluene which is inert under the reaction conditions.
  • the present invention also provides a second process in which a compound of formula I is produced, comprising reacting, in the presence of a transesterification catalyst, a piperidinol compound of formula V, as hereinbefore defined, with an ester having the formula:
  • R 3 and n have their previous significance and R 13 is an alkyl residue having from 1 to 4 carbon atoms, preferably 1 or 2 carbon atoms.
  • transesterification catalysts examples include alkali metal amides such as lithium amide.
  • a third process according to this invention in which a compound of formula I is produced comprises reacting, in the presence of an esterification catalyst, a pieridinol compound of formula V, as hereinbefore defined, with an acid having the formula:
  • esterification catalysts are neutral catalysts such as tetraalkyl titanates such as tetrabutyl titanate.
  • the second and third processes of the invention are conveniently effected by mixing the reactants together in the presence or absence of an inert solvent (for instance, benzene, toluene, xylene etc.) and agitating the reaction mixture until reaction is complete, as determined, for instance, by collecting the alcohol or water produced in the reaction, and stopping the reaction when the theoretical amount of alcohol or water, respectively, has been removed.
  • an inert solvent for instance, benzene, toluene, xylene etc.
  • a fourth process in which a compound of formula I is produced comprises reacting a compound having the formula: ##STR60## wherein R 2 , R 3 and n have their previous significance, with a compound X capable of reaction with the compound IX and of introducing into it the group R 1 as hereinbefore defined.
  • compound X may be an alkylating, alkenylating or aralkylating agent such as the halides of these groups.
  • Compound X may also be the aldehyde or ketone corresponding to the substituent R 1 , so that, when reacted with a compound of formula IX under Leuckart, Wallach or Eschweilar-Charles reaction conditions, compounds of formula I in which R 1 is methyl may be produced by reacting a compound of formula IX with formic acid and formaldehyde.
  • R 1 may be introduced before or after R 3 or in the case where R 1 and R 3 are identical may be introduced together by reacting a compound of the formula: ##STR62## with an alkylating, alkenylating, alkynylating, aralkylating, acylating agent or carbamoyloxyating agent, with an alkylating alkenylating, alkynylating, aralkylating or acylating agent.
  • Compounds of formula I wherein m is 1 and X 1 is --OH may be prepared by reacting a compound of formula XII with ethylene oxide, propylene oxide or styrene oxide.
  • R 1 represents an acyl group
  • R 2 and R 3 are as defined above
  • R 1 represents a carbamoyl or thiocarbamoyl group
  • R 2 and R 3 being as defined above with an isocyanate or thioisocyanate of the formula R 15 NCX 1 in which X 1 is ⁇ O or ⁇ S, and R 15 is the remainder of the isocyanate or thioisocyanate group.
  • R 2 in the general formula I is other than hydrogen it is preferred to introduce the appropriate group before or after the group R 1 is introduced, but before R 3 is introduced.
  • the group R 2 may be introduced by reacting a ketone of the formula ##STR76## wherein R 1 1 is hydrogen R 1 , with a Grignard reagent R 2 MgX followed by hydrolysis to produce a compound of the formula: ##STR77##
  • the acid binding agent can be an organic .Iadd.base .Iaddend.of an excess amount of the amine reactant XIV and the reactants are for example heated together in a solvent inert under the reaction conditions.
  • the process can be performed in the presence of a transesterification catalyst, such as an alkali metal, a piperidinol compound having the formula XIV, with an ester having the formula:
  • a transesterification catalyst such as an alkali metal, a piperidinol compound having the formula XIV, with an ester having the formula:
  • R and n are as defined above and R 16 is an alkyl group having from 1 to 4 carbon atoms, or with an acid having the formula:
  • R and n are as defined above.
  • the catalyst of producing compounds of the formula II can be a neutral catalyst such as tetraalkyl titanate.
  • the reactants can also be fused, the mass is agitated until reaction is complete and the reaction is stopped when the reaction is complete.
  • the completion of the reaction is determined for example by collecting, respectively, the alcohol or water produced in the reaction, and stopping the reaction when the theoretical amount of water or alcohol has been removed.
  • reaction can be effected in a solvent inert under the reaction conditions and in the presence of a strong base.
  • the present invention still further provides a composition comprising an organic material and a stabilising amount of a compound having the formula I, II or IV as hereinbefore defined.
  • the stabilisers of the invention provide effective light and/or heat stabilisation, especially for low- and high-density polyethylene and polypropylene and polystyrene as well as polymers of butene-1, pentene-1, 3-methyl-butene-1, hexane-1, 4-methylpentene-1, 4-methylhexene-1 and 4,4-dimethylpentene-1, and also co- and ter-polymers of olefines, particularly of ethylene or propylene.
  • organic materials susceptible to degradiation by the effects of light and the properties of which are improved by the incorporation therein of a compound of formula I, II or IV include natural and synthetic polymeric materials, for instance natural and synthetic rubbers, the latter including, for example, homo-, co- and ter-polymers of acrylonitrile, butadiene and styrene.
  • Specific synthetic polymers include polyvinyl chloride, polyvinylidene chloride and vinyl chloride co-polymers polyvinyl acetate as well as condensation polymers derived from ether, ester (derived from carboxylic sulphonic or carbonic acids), amide or urethane groupings. These polymers can, for instance, form the basis of surface coating media such as paints and lacquers having an oil or resin, for instance an alkyd or polyamide resin base.
  • the amount of the compound of formula I, II or IV, which is incorporated into the organic material in order to achieve maximal protection against degradation by light varies according to the properties of the organic material treated and according to the severity of the light radiation and to the length of exposure. However, for most purposes it is sufficient to use an amount of the compound of formula I, II or IV, within the range of from 0.01% to 5% by weight, more preferably within the range of from 0.1% to 2% by weight based on the weight of untreated organic material.
  • the compounds may be incorporated into the polymeric material by any of the known techniques for compounding additives with a polymer.
  • the compound and the polymer may be compounded in an internal mixer.
  • the compound may be added as a solution or slurry in a suitable solvent or dispersant, for instance an inert organic solvent such as methanol, ethanol or acetone to powdered polymer and the whole mixed intimately in a mixer, and the solvent subsequently removed.
  • the compound may be added to the polymer during the preparation of the latter, for instance at the latex stage of polymer production, to provide pre-stabilised polymer material.
  • the composition of the invention may contain one or more further additives, especially those used in polymer formulations, such as antioxidants of the phenol or amine type, U.V. absorbers and light protectants, phosphite stabilisers, peroxide decomposers, polyamide stabilisers, basic co-stabilisers, polyvinyl chloride stabilisers, nucleation agents, plasticizers, lubricants, emulsifiers, anti-static agents, flame-protectants, pigments, carbon black, asbestos, glass fibres, kaolin and talc.
  • further additives especially those used in polymer formulations, such as antioxidants of the phenol or amine type, U.V. absorbers and light protectants, phosphite stabilisers, peroxide decomposers, polyamide stabilisers, basic co-stabilisers, polyvinyl chloride stabilisers, nucleation agents, plasticizers, lubricants, emulsifiers, anti-static agents, flame-protectants, pigments, carbon black
  • the present invention therefore includes binary, tertiary and multi-component compositions containing the stabiliser of formula I, II or IV, together with one or more functional additives for polymers.
  • Suitable antioxidants are those of the hindered phenol type such as those selected from the following groups:
  • a 1 is --CR(COOR") 2 ##STR82##
  • R is hydrogen or lower alkyl, R' is lower alkyl,
  • R" is alkyl group having from 6-24 carbon atoms, w is an integer from 0 to 4.
  • Phenolic compounds having the formula: ##STR85## wherein B 1 , B 2 and B 3 are hydrogen, methyl or Q, provided that when B 1 and B 3 are Q then B 2 is hydrogen or methyl and when B 2 is Q then B 1 and B 3 are hydrogen or methyl.
  • R"' is a tetravalent radical selected from aliphatic hydrocarbons having from 1 to 30 carbon atoms, aliphatic mono- and di-thioethers having from 1 to 30 carbon atoms, aliphatic mono- and diethers having from 1 to 30 carbon atoms and z is an integer from 0 to 6.
  • Phenolic compounds having the formula ##STR88## where x is an integer of 1 or 2.
  • the preferred antioxidants consist of the hindered phenols in groups 1, 8, 9, 10, 11, 12 and 13 as mentioned above.
  • the most preferred hindered phenols are those of groups 1, 9, 11, 12 and 13.
  • antioxidants are those of the aminoaryl series for instance aniline and naphthylamine derivatives as well as their heterocyclic derivatives such as:
  • Ultraviolet absorbers and light protectants include
  • 2-(2'-hydroxyphenyl)benzotriazoles for instance 5'-methyl; 3',5'-di-t-butyl; 5'-t-butyl; 5-chloro-3', 5'-di-t-butyl; 5-chloro-3'-t-butyl-5'-methyl; 3'-sec.
  • 2-hydroxybenzophenones for instance the 4-hydroxy, 4-methoxy, 4-octoxy-, 4-decyloxy-, 4-dodecyloxy-, 4,2', 4'-trihydroxy or 2'-hydroxy-4,4'-dimethoxy derivatives.
  • 1,3-bis(2'-hydroxybenzoyl)-benzenes for instance, 1,3-bis-(2'-hydroxy-4'-hexyloxybenzoyl)benzene 1,3-bis-(2'-hydroxy-4'-octoxybenzoyl)benzene 1,3-bis-(2'-hydroxy-4'-dodecyloxybenzoyl)benzene
  • Aryl esters from optionally substituted benzoic acids such s phenylsalicylate, octylphenylsalicylate, dibenzoyl resorcino, bis-(4-tert.butylbenzoyl) resorcinol, benzoylresorcinol and 3,5-di-tert.butyl-4-hydroxybenzoic acid-2,4-di-tert.butyl phenyl ester and -octadecyl ester and -2-methyl-4,6-di-tert.butyl phenyl ester.
  • Nickel compounds such as nickel complexes of 2,2'-thio-bis-(4-tert.octylphenol), for instance the 1:1 and 1:2 complexes, optionally having other ligands such as n-butylamine, triethanolamine or N-cyclohexyl-diethanolamine; nickel complexes of bis-(4-tert.octylphenyl) sulphone such as the 2:1 complex, optionally having other ligands such as 2-ethylcaproic acid; nickel dibutyl di-thiocarbamates; nickel salts of 4-hydroxy-3,5-di-tert.
  • Nickel compounds such as nickel complexes of 2,2'-thio-bis-(4-tert.octylphenol), for instance the 1:1 and 1:2 complexes, optionally having other ligands such as n-butylamine, triethanolamine or N-cyclohexyl-diethanolamine; nickel complexes of bis-(4-tert.octy
  • butylbenzyl-phosphonic acid mono-alkyl esters such as the methyl-, ethyl- or butyl esters; the nickel complex of 2-hydroxy-4-methyl-phenyl-undecylketonoxime; and nickel-3,5-di-tert.butyl-4-hydroxy benzoate, and
  • Phosphite stabilisers include triphenyl phosphite, diphenylalkyl phosphites, phenyl dialkyl phosphites, trinonylphenyl phosphite, trilauryl phosphite, trioctadecyl phosphite, 3,9-di-isodecyloxy-2,4,8,10-tetraoxa-3,9-diphosphaspiro-(5,5)-undecane and tri-(4-hydroxy-3,5-di-tert.butylphenyl)phosphite.
  • Peroxide-decomposing compounds for polyolefins include esters of ⁇ -thiodipropionic acids, for instance the lauryl-, stearyl-, myristyl- or tridecyl esters, salts of mercaptobenzimidazoles such as the zinc salt and diphenylthiourea.
  • Suitable polyamide stabilisers include copper salts in combination with iodides and/or further phosphorus compounds and salts of bivalent manganese.
  • Basic co-stabilisers are, for example, polyvinylpyrrolidone, melamine, benzoguanamine, triallyl cyanurate, dicyandiamide, urea derivatives, hydrazine derivatives, amines, polyamides, polyurethanes, alkali and alkaline earth salts of higher saturated or unsaturated fatty acids such as calcium stearate.
  • Polyvinyl chloride stabilisers include organotin compounds, organo lead compounds and Ba/Cd salts of fatty acids.
  • nucleation agents examples include 4-tert.butyl benzoic acid, adipic acid and diphenylacetic acid.
  • any further additive is advantageously employed in a proportion within the range of from 0.01% to 5% by weight, based on the weight of untreated polymeric material.
  • the compounds of formula I, II or IV provide very effective stabiliser packages in polyolefine formulations.
  • Table 2 gives a list of esters prepared using the procedure of Example 34.
  • Table 3 gives a list of carbamoyloxy esters prepared using the procedure of Example 45.
  • Table 5 gives a list of ethers prepared using the procedure of Example 70.
  • Table 6 gives a list of compounds prepared using the procedure of Example 77.
  • This composition was compression moulded into films of 0.1 mm thickness at 260° C. for 6 minutes and the films so obtained were then quenched in cold water.
  • a section measuring 44 ⁇ 100 mm was separated from the 0.1 mm annealed polypropylene foil and exposed to light irradiation in a fademeter device consisting of a circular bank of 28 alternate sunlight and blacklight lamps.
  • the sunlight lamps were 2 feet long, 20-watt fluorescent lamps characterised by a peak emission of 3,100 Angstrom units; the blacklight lamps were 2 feet long, 20-watt ultraviolet lamps characterised by a peak emission of 3,500 Angstrom units.
  • the sample was rotated concentrically about the bank of lamps so that the radiation therefrom was uniformly distributed over the section under test.
  • the exposed sample was examined periodically and portions of it tested for the percent/elongation at break, the time at which the sample reached 50% of the initial elongation at break was noted.
  • the pressing was conducted at 180° C. and the pressings were compression-moulded into 1 mm. thick plaques at 150° C.
  • the plaques were stored at 20° C. and were periodically examined visually for the first sign of exudation.
  • the T.sub.(560) represents the transmission value of an unexpected sample at a wavelength of 560 .[.m.]..Iadd.n.Iaddend.m.
  • 25 parts by weight of a polyester-based film-forming polyurethane were dissolved in 75 parts by weight of a 1:1 mixture (by volume) of dimethylformamide and acetone, and 1% by weight of 4(2'-cyanoethoxy)-1,2,2,6,6-pentamethylpiperidine was added.
  • the final thickness of the film was 80-100 ⁇ .
  • the dried film samples were removed from the glass plate, mounted on white cardboard and exposed in a "Xenotest 450" exposure unit, one half of the exposed sample being covered to facilitate subsequent visual estimation of yellowing due to exposure.
  • the sample was controlled and rated visually at intervals of 100 hours.
  • the multifilament obtained was mounted on a sample holder of Xenotest 150 apparatus (Quarzlampen GmbH) using white cardboard as backing. In intervals of 200 hours of exposure time, 5 fiber samples are measured for their retained tensile strength. The data obtained are plotted against exposure time and the exposure time (T) to give 50% loss or original tensile strength is derived from graph. This value is taken as the failure time.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Materials Engineering (AREA)
  • Hydrogenated Pyridines (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

New 1- and 4-substituted piperidines are stabilizers for organic material. They are produced by reacting corresponding 1-substituted piperidinols with acid chlorides or corresponding 4-substituted piperidines with a compound introducing into the 1-position a residue.

Description

This is a continuation of application Ser. No. 310,031 filed Nov. 28, 1972, now abandoned.
The present invention relates to new piperidine derivatives, and in particular to new piperidine derivatives substituted at the 1- and 4- positions and having value as stabilisers for polymeric materials.
In German Patent Specification No. 1,929,928 there are described compounds having the general formula: ##STR1## wherein R1 ' and R2 ' are the same or different and each is an alkyl group, or, together with the carbon atom to which they are bound, they form a saturated alicyclic group or a group having the formula: ##STR2## n' is a whole number from 1 to 3 inclusive; and when n' is 1, .[.R3 .]. .Iadd.R3 '.Iaddend. is an acyl group derived from an aliphatic, alicyclic or heterocyclic mono-carboxylic acid, an N-substituted carbamoyl group derived from an N-substituted carbamic acid, an N-substituted thiocarbamoyl group derived from an N-substituted thiocarbamic acid, a monovalent group obtained by removing an hydroxyl group from an oxo-acid, an alkyl group, a cycloalkyl group, an aralkyl group, an aryl group or a group having the formula: ##STR3## wherein R1 ' and R2 ' have their previous significance; when n' is 2, R2 is a diacyl group derived from an aliphatic, alicyclic, aromatic or heterocyclic dicarboxylic acid, a dicarbamoyl group derived from a dicarbamic acid, a bis-thiocarbamoyl group derived from a bis-thiocarbamic acid, a carbonyl group, a divalent group obtained by removing two hydroxyl groups from an oxo-acid, an alkylene group, an arylene group, or an arylenedialkylene group; and when n' is 3, .[.R3 .]. .Iadd.R3 '.Iaddend. is a triacyl group, derived from an aliphatic, alicyclic, aromatic or heterocyclic tricarboxylic acid, a tricarbamoyl group derived from tricarbamic acid, a tris-thiocarbamoyl group derived from a tris-thiocarbamic acid, a trivalent group obtained by removing three hydroxyl groups from an oxo-acid, an alkanetriyl group, arenetriyl group or an arenetriyl trialkylene group.
We have now found that certain piperidine derivatives substituted in the 1- and 4- positions are effective stabilisers for polymers, especially against photo- and thermal degradation.
According to the present invention, there is provided a compound having the formula: ##STR4## and their salts wherein n is 1, 2, 3 or 4; R1 is a monovalent residue and is an alkyl residue having from 1 to 20, preferably 1 to 12 carbon atoms, an alkenyl or alkynyl residue having from 3 to 20, preferably 3 to 12 carbon atoms, an aralkyl residue having from 7 to 12 carbon atoms, or a residue having the formula: ##STR5## wherein m is 1, 2 or 3; R4 is hydrogen, methyl or phenyl residue, X2 is halogen, cyano, ##STR6## --COR5, --CO.OR5, --CO.SR5, or --CONR5 R6 and X1 is hydroxyl, halogen, cyano, --OR5, ##STR7## wherein R5 is an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 2 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an aryl residue having from 6 to 11 carbon atoms, an aryl residue having from 6 to 11 carbon atoms or an aralkyl residue having 7 to 11, preferably 7 to 8 carbon atoms when R5 is joined to a nitrogen atom, also hydrogen and R6 is preferably hydrogen or an alkyl residue having from 1 to 4 carbon atoms, or R5 and R6 together with the nitrogen atom to which they are bound form a 5- or 6-membered ring which contains no other heteroatoms or contains one or more other heteroatoms, or R1 is an acyl group ##STR8## wherein R7 is hydrogen, an unsubstituted aliphatic or substituted aliphatic residue having from 1 to 20 carbon atoms, an alkenyl or alkynyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, an aromatic residue having from 6 to 20, preferably 6 to 12, carbon atoms or an heterocyclic residue, or R1 is a carbamoyl or thiocarbamoyl residue having the formula: ##STR9## wherein X3 is --O-- or --S--, R8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, and R9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an unsubstituted aryl or substituted aryl residue having from 6 to 12 carbon atoms; R2 is an alkyl residue having from 1 to 4 carbon atoms, an alkenyl or alkynyl residue having 3 to 20 carbon atoms, preferably 3 or 4 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an aryl residue having from 6 to 11 carbon atoms or an aralkyl residue having from 7 to 9 carbon atoms or preferably hydrogen; and when n is 1, R3 is a monovalent radical having the same significance as R1, or R3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorous containing acid or a boric acid, or R3 is an aryl residue, a cycloalkyl group having from 5 to 12 carbon atoms, or a residue having the formula: ##STR10## wherein R1 ' is hydrogen or R1 ' has the same significance as R1 :
When n is 2, R3 is a divalent residue and is an alkylene residue having from 1 to 20 carbon atoms, an alkenylene residue having from 2 to 20, preferably 3 to 20, carbon atoms, an alkynylene residue having from 2 to 20, preferably 3 to 20, carbon atoms, cycloalkylidene residue having from 5 to 12 carbon atoms, an arylene residue having 6 to 14 carbon atoms, an aralkylene residue having from 8 to 14 carbon atoms or an aliphatic, aromatic or heterocyclic diacyl residue, ##STR11## an aliphatic or aromatic dicarbamoyl or dithiocarbamoyl residue, sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or a boric acid.
When n is 3, R3 is a trivalent residue and is an .[.arenetriyl.]. .Iadd.alkanetriyl .Iaddend.or an arenetriyl-trialkylene residue, an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric, o-phosphorous or o-boric acid; and
when n is 4, R3 is a tetravalent residue and is an alkane tetrayl residue, or a tetraacyl residue derived from an aliphatic or aromatic tetracarboxylic acid or from o-silicic acid;
as well as, when n is 2, 3 or 4, partial ethers, esters and carbamoyloxy and thiocarbamoyloxy compounds related to the fully-reacted compounds of formula I.
When n is 1, R1 and/or R3 may be an alkyl residue having from 1 to 20 carbon atoms, preferred 1 to 18, examples of this substituent are methyl, ethyl, n-propyl, n-butyl, sec-butyl, t-butyl, n-hexyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-hexadecyl or n-octadecyl residue and eicosyl. In terms of accessibility and activity however for optimal compatibility with polyolefines substrates, alkyl substitutents R1 and/or R3 having from 5 to 20, especially 5 to 12 carbon atoms are preferred. A sub-group of alkyl residues R1 is that containing from 1 to 4 carbon atoms, preferably methyl.
In those cases in which R1 and/or R3 is an alkenyl residue having from 3 to 20 carbon atoms, examples of these substituents are allyl, methallyl, 3-hexenyl, 4-octenyl, 6-decenyl, 10-undecenyl, and8-octadecenyl residues, however the preferred substituents in this group are allyl and methallyl residues.
When the residues R1 and/or R3 are alkynyl they may be for example propargyl, but-1- and -2-ynyl, pent-1-ynyl, hex-1-ynyl, oct-1-ynyl, dec-1-ynyl, dodec-1-ynyl, tetradec-1-ynyl and octadec-1-ynyl. The preferred alkynyl substituents however are propargyl and methylpropargyl.
When R1 and/or R3 is an aralkyl residue, suitable examples are benzyl, β-phenethyl, α-methylbenzyl, αα-dimethylbenzyl, α-naphthylmethyl and p-methyl-α-methylbenzyl residues. Benzyl is preferred.
A further sub-group of R1 and/or R3 substituents is substituted alkyl derivatives having the formula: ##STR12## wherein m, R4, X1 and X2 have their previous significance, but wherein, however, R4 is preferably hydrogen and m is preferably 1.
When X1 is an hydroxyl residue, examples of this substituents R1 and/or R3 are 2-hydroxyethyl, 2- and 3-hydroxypropyl, 3- and 4-hydroxybutyl, 4-hydroxypentyl and 2-hydroxy-2-phenyl ethyl, preferably 2-hydroxyethyl, 2-hydroxypropyl and 2-hydroxy-2-phenylethyl.
When X1 and/or X2 are halogen atoms, examples of R1 and/or R3 include 2-chloro- and 2-bromo ethyl, 2- and 3-chloro- and 2- and 3-bromopropyl, 3- and [4-chorobutyl and 2-chloro-2-phenyl ethyl, preferably 2-choroethyl, 2-chloropropyl and 2-chloro-2-phenylethyl.
When X1 and/or X2 are cyano groups, R1 and/or R3 include cyanomethyl, 1- and 2- cyanobutyl, 4-cyanopentyl, 2-cyano-2-phenylethyl groups, preferably a 2-cyanoethyl group.
When X2 is a 1,2-epoxy group, R1 and/or R3 may be 2,3-epoxy-n-propyl, 2,3 -epoxy-methylpropyl, but the preferred epoxyalkyl substituent is 2,3 -epoxy-n-propyl.
When X1 is --OR5, --OCOR5, --OCSR5, --OCONR6 R5, --CSNR6 R5, or when X1 and/or X2 are --COR5, --COOR5, --COSR5, --CONR6 R5 and the group R5 is alkyl, then the alkyl group preferably has from 1 to 12, most preferred 1 to 2, carbon atoms; when R5 is an alkenyl residue, then it preferably contains 2 to 4 carbons; when R5 is a cycloalkyl group it preferably contains 6 carbon atoms; when R5 is an aryl residue it preferably contains 6 or 7 carbons; and when R5 is an aralykyl residue, it preferably has 7 or 8 carbon atoms.
R5 and R6 together with the nitrogen atom to which they are bound can form a 5- or 6-membered ring such as the pyrrolidinyl-, imidazolidinyl-, pyrazolidinyl-, piperidinyl-, piperazinyl- or morpholinyl ring.
Examples of R1 and/or R3 within this sub-group ae 2-methoxyethyl, 2-ethoxyethyl, 2-propoxyethyl, 2-butoxyethyl, 2-methoxypropyl, 2- and 3-ethoxypropyl, 2- and 3-n-butoxypropyl, 3- and 4-methoxybutyl, 3- and 4-ethoxybutyl, 3- and 4-butoxybutyl, 4-methoxypentyl, 4-ethoxypentyl, 4-n-butoxypentyl, 2-methoxy-2-phenyl ethyl, 2-ethoxy-2-phenyl ethyl; 2-acetoxyethyl, 2-n-propionoxyethyl, 2-benzoyloxy ethyl, 2-acetoxypropyl, 2-n-propionoxypropyl, 4-acetoxybutyl, 4-n-propionoxybutyl, 4-acetoxypentyl, 4-n-propionoxypentyl, 2-phenyl-2-acetoxyethyl, 2-(methylcarbamoyloxy) ethyl, 2-ethylcarbamoyloxy)ethyl, 2-(phenylcarbamoyloxy) ethyl, 2-(methylcarbamoyloxy) propyl, 2-(ethylcarbamoyloxy) propyl, 2-phenyl-2-(carbamoyloxy) ethyl, 2-(allylthiocarbamoyloxy) ethyl, 2-phenyl-2-(methylcarbamoyloxy) ethyl, 2-phenyl-2-(phenylcarbamoyloxy) ethyl, methylcarbonylmethyl, 2-(methylcarbonyl) ethyl, 2-(ethyl-carbonyl) ethyl, 2-(methylcarbonyl) propyl, and 2-(methylcarbonyl)-2-phenyl ethyl; methoxycarbonyl methyl, 2-(ethoxycarbonyl) ethyl, 2-(methoxycarbonyl)-propyl, and 2-(methoxycarbonyl)-2-phenylethyl, 2-(ethylthiocarbonyl) ethyl, 2-(methylthiocarbonyl) propyl and 2-(methylthiocarbonyl)-2-phenylethyl; carbamoylmethyl, 2-carbamoylethyl, 2-methylcarbamoylethyl, 2-ethylcarbamoylethyl, dimethylcarbamoylmethyl, 2-diethylcarbamoylethyl, thiocarbamoylmethyl, 2-(thiocarbamoyl) ethyl, 2-methylthiocarbamoylethyl, dimethylthiocarbamoylmethyl, 2-(phenylcarbamoyl) ethyl.
When n is 1 and R1 and/or R3 is an acyl group --COR7 wherein R7 is an unsubstituted aliphatic or substituted aliphatic residue having from 1 to 20, preferably 1 to 19, carbon atoms, R7 may be a methyl, ethyl, propyl, butyl, hexyl, n-octyl, 2-ethylhexyl, n-decyl, n-undecyl, n-tridecyl, n-tetradecyl, n-hexadecyl, n-heptadecyl and eicosyl, chloroethyl, chlorohexyl, methylthioethyl, ethylthioethyl, octylthioethyl, or dodecylthioethyl residue; alkenyl residues R7 have from 2 to 20, preferably 2 to 17, most preferred 2 to 6, carbon atoms such as vinyl, allyl, methallyl, isobutenyl or hexenyl group; alkynyl residues R7 have from 2 to 20, preferably 2 to 6, carbon atoms such as a propargyl group; cycloaliphatic residues R7 have from 5 to 12, preferably 6 to 10, most preferred 6, carbon atoms such as a cyclopentyl or cyclohexyl residue; araliphatic residues R7 have from 7 to 14, preferably 7 to 13, most preferred 7 to 9, carbon atoms such as a benzyl, β-phenylethyl, diphenylmethyl or styryl residue; unsubstituted aromatic residues R7 have from 6 to 14, preferably 6 to 10, carbon atoms such as a phenyl or naphthyl residue, a substituted aromatic residue, substituted by for example alkyl having 1 to 4 carbon atoms such as tolyl, p-tertbutylphenyl; and heterocyclic residues R7 may be a furan or thiophene residue. Examples of compounds wherein R1 and/or R3 are unsaturated acyl groups are preferred those wherein only one of R1 and R3 denotes an unsaturated acyl group.
Examples of acyl groups R1 and/or R3 are formyl, acetyl, propionyl, n-butyryl, hexanoyl, heptanoyl, octanoyl, 2-ethylhexanoyl, 2,2,4-trimethylpentanoyl, n-decanoyl, n-dodecanoyl, n-tetradecanoyl, n-hexadecanoyl, n-octadecanoyl, n-eicosoyl, acryloyl, α-methacrylol, crotonoyl, undec-10-enoyl, octadec-9-enoyl, β-methylthiopropionyl, methylthioacetyl, β-octylthiopropionyl, β-dodecylthiopropionyl, cyclopentanoyl, cyclohexanoyl, benzoyl, α- and β-naphthoyl cyclopentylacetyl, cyclohexylacetyl, phenylacetyl, β-phenylpropionyl, diphenyloctyl, β-phenylacryloyl, o-, m- and p-toluoyl, o-, m- or p-methoxybenzoyl and o-, m- and p-chlorobenzoyl, 2-furoyl and 2-picolinoyl.
When n is 1, R1 and/or R3 may also be a carbamoyl or thiocarbamoyl residue having the formula: ##STR13## wherein X3 is --O-- or --S--, R8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms and R9 is hydrogen, an alkyl residue having from 1 to 20, preferably 1 to 8, carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an unsubstituted .[.alkyl.]. .Iadd.aryl.Iaddend., or substituted aryl, for instance, alkyl or halogen-substituted aryl residue having from 6 to 12, preferably 6 to 10, carbon atoms. Examples of suitable residues within this group are carbamoyl, N-methylcarbamoyl, N-ethyl-carbamoyl, N-n-propylcarbamoyl, N-isopropylcarbamoyl, N-n-butylcarbamoyl, N-n-pentylcarbamoyl, N-n-octylcarbamoyl, N-n-decylcarbamoyl, N-n-dodecylcarbamoyl, N-n-octadecyl, N-n-eisocylcarbamoyl, N-allylcarbamoyl, N-methallylcarbamoyl, N-undecenylcarbamoyl, N-cyclopentylcarbamoyl, N-cyclohexylcarbamoyl, N-methylcyclohexylcarbamoyl, N-cyclododecylcarbamoyl, N-(1- and 2-perhydronaphthyl)-carbamoyl, N-adamantylcarbamoyl, N-cyclopentylmethylcarbamoyl, N-benzylcarbamoyl N-(β-phenethyl)carbamoyl, N-(1- and 2-naphthylmethyl) carbamoyl, N-phenylcarbamoyl, N-(o-, m- and p-tolyl)carbamoyl, N-(2,4- and 2,6-xylyl)carbamoyl, N-(α-and β-naphthyl)carbamoyl, N,N-dimethylcarbamoyl, N-methyl, N-ethylcarbamoyl, N,N-diethylcarbamoyl, N,N-diisopropylcarbamoyl, N,N-di-n-propylcarbamoyl, N,N-di-n-butyl-carbamoyl and N,N-di-isobutylcarbamoyl residues as well as the corresponding thiocarbamoyl residues.
When R2 is an alkyl residue it is for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, preferably methyl, as alkenyl residue R2 is for example allyl, methallyl, 3-hexenyl, 4-octenyl, 6-decenyl, 10-undecenyl or 8-octadecenyl, peferably allyl or methallyl and as alkynyl residue for example propargyl, but-1- and -2-ynyl, penta-1-ynyl, hex-1-ynyl, oct-1-ynyl, dec-1-ynyl, dodec-1-ynyl, tetradec-1-ynyl and octadec-1-ynyl, preferably propargyl, R2 as cycloalkyl is for example cyclopentyl, cyclohexyl, cyclooctyl, cyclododecyl, preferably cyclohexyl as aryl residue R2 is for example phenyl, p-tolyl, t-butylphenyl, naphthyl, preferably phenyl or p-tolyl and as aralkyl residue it is for example benzyl, alpha-methylbenzyl, p,alphadimethylbenzyl, preferably benzyl.
When n is 1
R3 may be the same as R1. If R3 is alkyl it is preferably an alkyl group having from 3 to 18 carbon atoms.
When R3 represents an aryl residue it is for example an aromatic residue having 6 to 20 carbon atoms, preferably an aryl residue having 6 to 12 carbon atoms, most preferred phenyl.
When n is 2
R3 is, for example an alkylene residue having from 1 to 20, preferably 2 to 6, carbon atoms such as methylene, ethylene, trimethylene, tetramethylene or hexamethylene residue. Alkenylene residues R3 preferably contain 3 to 20, most preferred 3 or 4 carbons, and may be, for instance a 1,3-propen-ene or 1,4-buten-2-ene residue. Alkynylene residues R3 preferably contain 3 to 20, most preferred 4 carbon atoms and may be, for instance a 1:4 but-2-ynylene residue. When R3 is a cycloalkylidene residue, it preferably contains 7 or 8 carbon atoms, for instance a cyclohexyldimethylene residue.
When R3 is arylene it has preferably 6 to 12 carbon atoms and it may be for example 1,3-phenylene, or 4,4'-diphenylene.
When R3 is aralkylene it may be for example α,α-p-xylylene.
Diacyl residues R3 include those derived from an aliphatic, aromatic or heterocyclic dicarboxylic acid. Examples of aliphatic dicarboxylic acids are those having from 2 to 20, preferably alkan dicarboxylic acids having 6 to 10 carbon atoms such as malonic, succinic, glutaric, adipic, pimelic, suberic, azelaic, sebacic, 1,12-dodecanedioic, 1,18 -octadecanedioic, 1,20-docosanedioic acid and N-methyliminodiacetic acid. Examples of aromatic diacyl residues are those derived from phthalic, isophthalic and terephthalic acids, each optionally ring-substituted, for instance by halogen, an alkyl or alkoxy group each having from 1 to 20 carbon atoms, a hydroxy or tertiary amino group.
Examples of heterocyclic dicarboxylic acids are 2,5-thiophene dicarboxylic acid or 2,5-furandicarboxylic acid.
R3 is for example an aliphatic or aromatic dicarbamoyl residue such as a divalent .[.alkyl.]. .Iadd.alkylene .Iaddend.dicarbamoyl residue for example the divalent residue of butan-1,4-dicarbamoyl or hexan-1,6-dicarbamoyl or such as a divalent .[.aryl.]. .Iadd.arylene .Iaddend.dicarbamoyl residue such as the divalent residue of .[.phenyl.]. .Iadd.phenylene.Iaddend.-1,4-dicarbamoyl. R3 is for example an aliphatic or aromatic dithicarbamoyl residue such as a divalent .[.alkyl.]. .Iadd.alkylene .Iaddend.dithicarbamoyl residue for example the divalent residue of butan-1,4-dithiocarbamoyl or hexan-1,6-dithiocarbamoyl or such as an divalent .[.aryl.]. .Iadd.arylene .Iaddend.dithiocarbamoyl residue sue as the divalent residue of .[.phenyl.]. .Iadd.phenylene.Iaddend.-1,4-dithiocarbamoyl.
When n is 3
R3 is, for instance, a triacyl group derived from an aliphatic tricarboxylic acid such as nitrilotriacetic acid, tricarballylic acid, from an aromatic tricarboxylic acid such as benzene tricarboxylic acid or from an inorganic acid such as o-phosphorous, o-phosphoric or o-boric acid, or oxyacids, for example, benzene-1,3,5-trisulphonic acid.
When n is 4
R3 is, for instance, a tetracyl group derived from a tetracarboxylic acid, such as ethylene diamine, tetracarboxylic acid, from the tetracarboxylic acids described in British Patent Specification No. 1080335, 1,2,4,5,-benzene tetracarboxylic acid or from o-silicic acid.
R3 preferably represents an acyl or an N- substituted carbamoyl, an alkylene group, a substituted alkylene or an aralkyl group.
R1 preferably represents an alkyl, alkenyl, or substituted alkyl group such as hydroxyalkyl, alkylcarbonyloxy or aralkyl group.
Examples of compounds of the present invention are:
Examples where n=1
4-Methoxy-1,2,2,6,6-pentamethylpiperidine
4-n-Butoxy-1,2,2,6,6-pentamethylpiperidine
4-n-Dodecyloxy-1,2,2,6,6-pentamethylpiperidine
4-n-Octadecyloxy-1,2,2,6,6-pentamethylpiperidine
4-(2'-Cyanoethoxy)-1,2,2,6,6-pentamethylpiperidine
4-(2'-Hydroxyethoxy)-1,2,2,6,6,-pentamethylpiperidine
1-n-Propyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1-n-Propyl-4-n-dodecyloxy-2,2,6,6,-tetramethylpiperidine
1-n-Propyl-4-n-octadecyloxy-2,2,6,6-tetramethylpiperidine
1-sec-Butyl-4-n-dodecyloxy-2,2,6,6-tetramethylpiperidine
1-n-Octyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1-n-Dodecyl-4-n-dodecyloxy-2,2,6,6-tetramethylpiperidine
1-n-Octadecyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1-n-Octadecyl-4-n-octadecyloxy-2,2,6,6-tetramethylpiperidine
1-n-Eicosyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1-Allyl-4-methoxy,2,2,6,6-tetramethylpiperidine
1-Allyl-4-allyloxy-2,2,6,6-tetramethylpiperidine
1-(1'-Undec-10'-enyl)-4-n-butoxy-2,2,6,6-tetramethylpiperidine
1-(1'-Undec-10'-enyl)-4-(1'-undec-10'-enyloxy)-2,2,6,6-tetramethylpiperidine
1-Oleyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1-Oleyl-4-oleyloxy-2,2,6,6-tetramethylpiperidine
1-Propargyl-4-ethoxy-2,2,6,6-tetramethylpiperidine
1-Propargyl-4-propargyloxy-2,2,6,6-tetramethylpiperidine
1-Benzyl-4-n-dodecyloxy-2,2,6,6-tetramethylpiperidine
1-Benzyl-4-allyloxy-2,2,6,6-tetramethylpiperidine
1-Benzyl-4-propargyloxy-2,2,6,6-tetramethylpiperidine
1-Benzyl-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-Hydroxyethyl)-4-methoxy-2,2,6,6-tetramethylpiperidine
1-(2'-Hydroxypropyl)-4-allyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-Hydroxyethyl)-4-propargyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-Hydroxypropyl)-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-Hydroxyethyl)-4-(2'-hydroxyethoxy)-2,2,6,6-tetramethylpiperidine
1-(2'-Hydroxypropyl)-4-(2'-hydroxypropoxy)-2,2,6,6-tetramethylpiperidine
1-(2'-Hydroxy-2'-phenylethyl)-4-n-butoxy-2,2,6,6-tetramethylpiperidine
1-(2'-Hydroxy-2'-phenylethyl)-4-(2'-hydroxy-2'-phenylethoxy)-2,2,6,6-tetramethylpiperidine
1-(2'-Chloroethyl)-4-n-docecyloxy-2,2,6,6-methylpiperidine
1-(2'-Chloropropyl) -4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-Bromoethyl)-4-(2'-bromoethoxy- 2,2,6,6-tetramethylpiperidine
1-(2'-Chloro-2'-phenylethyl)-4-n-octyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-Cyanoethyl)-4-phenoxy-2,2,6,6-tetramethylpiperidine
1-(2'-Cyanoethyl)-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-Cyanoethyl)-4-(2'-cyanoethoxy)-2,2,6,6-tetramethylpiperidine
1-(2'-Cyanopropyl)-4-methoxy-2,2,6,6-tetramethylpiperidine
1(2',3'-.[.epoxypropyl).]..Iadd.Epoxypropyl).Iaddend.-4-n-butoxy-2,2,6,6-tetramethylpiperidine
1-(2',3'-.[.epoxypropyl).]..Iadd.Epoxypropyl).Iaddend.-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1(2',3'-.[.epoxypropyl).]..Iadd.Epoxypropyl).Iaddend.-4-(2',3'-epoxypropoxy)-2,2,6,6-tetramethylpiperidine
1-(2'-.[.methoxyethyl).]..Iadd.Methoxyethyl).Iaddend.-4-ethoxy-2,2,6,6-tetramethylpiperidine
1-(2'-.[.methoxyethyl).]..Iadd.Methoxyethyl).Iaddend.-4-(2'-methoxyethoxy)-2,2,6,6-tetramethylpiperidine
1-(2'-.[.ethoxypropyl).]..Iadd.Ethoxypropyl).Iaddend.-4-allyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-.[.ethoxy.]..Iadd.Ethoxy.Iaddend.-2'-phenylethyl)-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-.[.acetoxyethyl).]..Iadd.Acetoxyethyl).Iaddend.-4-n-butoxy-2,2,6,6-tetramethylpiperidine
1-(2'-.[.benzoyloxyethyl).]..Iadd.Benzoyloxyethyl).Iaddend.-4-(2'-benzoyloxyethoxy)-2,2,6,6-tetramethylpiperidine
1-(2'-.[.propionoxypropyl).]..Iadd.Propionoxypropyl).Iaddend.-4-allyloxy-2,2,6,6-tetramethylpiperidine
1-[2'-.[.(methylcarbamoyloxy).]..Iadd.(Methylcarbamoyloxy).Iaddend.ethyl]-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-[2'-.[.(methylcarbamoyloxy).]..Iadd.(Methylcarbamoyloxy).Iaddend.ethyl]-4-[2'-(methylcarbamoyloxy)ethyoxy]-2,2,6,6-tetramethylpiperidine
1-[2'-(Phenylcarbamoyloxy)ethyl]-4-[2'-cyanoethoxy]-2,2,6,6-tetramethylpiperidine
1-[2'-.[.(ethylthiocarbamoyloxy).]..Iadd.(Ethylthiocarbamoyloxy).Iaddend.ethyl]-4-[2'-(ethylthiocarbamoyloxy)ethoxy]-2,2,6,6-tetramethylpiperidine
1-Methylcarbonylmethyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1-[.[.(methylcarbonyl).]..Iadd.(Methylcarbonyl).Iaddend.ethyl]-4-n-octyloxy-2,2,6,6-tetramethylpiperidine
1-Methylcarbonylmethyl-4-methylcarbonylmethoxy-2,2,6,6-tetramethylpiperidine
1-(2'-.[.methoxycarbonylethyl).]..Iadd.Methoxycarbonylethyl).Iaddend.-4-(2'-methoxycarbonylethoxy)-2,2,6,6-tetramethylpiperidine
1-(2'-.[.methoxycarbonylethyl).]..Iadd.Methoxycarbonylethyl).Iaddend.-4-ethoxy-2,2,6,6-tetramethylpiperidine
1-[2'-.[.(ethoxycarbonyl).]..Iadd.(Ethoxycarbonyl).Iaddend.ethyl]-4-(2'-hydroxyethoxy)-2,2,6,6-tetramethylpiperidine
1-[2'-.[.(thioethoxycarbonyl).]..Iadd.(Thioethoxycarbonyl).Iaddend.ethyl]-4-methoxy-2,2,6,6-tetramethylpiperidine
1-Carbamolymethyl-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-(2'-Carbamoylethyl-4-dodecoxy-2,2,6,6-tetramethylpiperidine
1-[2'-(Methylcarbamoyl)ethyl]-4-[2'-methylcarbamoylethoxy]-2,2,6,6-tetramethylpiperidine
1-[2'-(Diethylcarbamoyl)ethyl]-4-methoxy-2,2,6,6-tetramethylpiperidine
1-Thiocarbamoylmethyl-4-allyloxy-2,2,6,6-tetramethylpiperidine
1-(Dimethylthiocarbamoyl)methyl-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-Acetyl-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-Lauroyl-4-(2'-hydroxyethoxy)-2,2,6,6-tetramethylpiperidine
1-Stearoyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1-Benzoyl-4-n-butoxy-2,2,6,6-tetramethylpiperidine
1-Carbamoyl-4-n-octadecyloxy-2,2,6,6-tetramethylpiperidine
1-Methylcarbamoyl-4-benzyloxy-2,2,6,6-tetramethylpiperidine
1-Phenylcarbamoyl-4-(2'-hydroxyethoxy)-2,2,6,6-tetramethylpiperidine
1-Phenylthiocarbamoyl-4-(cyclohexyloxy)-2,2,6,6-tetramethylpiperidine
1-Dimethylcarbamoyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1-Methylthiocarbamoyl-4-n-octyloxy-2,2,6,6-tetramethylpiperidine
1-Phenylthiocarbamoyl-4-methoxy-2,2,6,6-tetramethylpiperidine
1,2,2,6,6-Pentamethylpiperidinyl-4-formate
1,2,2,6,6-Pentamethylpiperidinyl-4-acetate
1,2,2,6,6-Pentamethylpiperidinyl-4-isobutyrate
1,2,2,6,6-Pentamethylpiperidinyl-4-n-octanoate
1,2,2,6,6-Pentamethylpiperidinyl-4-pivalate
1,2,2,6,6-Pentamethylpiperidinyl-4-stearate
1,2,2,6,6-Pentamethylpiperidinyl-4-eicosanoate
1,2,2,6,6-Pentamethylpiperidinyl-4-(2'-ethylhexanoate)
1,2,2,6,6-Pentamethylpiperidinyl-4acrylate
1,2,2,6,6-Pentamethylpiperidinyl-4-oleate
1,2,2,6,6-Pentamethylpiperidinyl-4-cyclohexanecarboxylate
1,2,2,6,6-Pentamethylpiperidinyl-4-adamantane-1-carboxylate
1,2,2,6,6-Pentamethylpiperidinyl-4-benzoate
1,2,2,6,6-Pentamethylpiperidinyl-4-p-toluate
1,2,2,6,6-Pentamethylpiperidinyl-4-p-t-butylbenzoate
1,2,2,6,6-Pentamethylpiperidinyl-4-p-methoxybenzoate
1,2,2,6,6-Pentamethylpiperidinyl-4-o-chloro-benzoate
1,2,2,6,6,-Pentamethylpiperidinyl-4-p-chloro-benzoate
1,2,2,6,6,-Pentamethylpiperidinyl-4α-naphthoate
1,2,2,6,6,-Pentamethylpiperidinyl-4-phenylacetate
1,2,2,6,6,-Pentamethylpiperidinyl-4-(1'-napthylacetate)
1,2,2,6,6,-Pentamethylpiperidinyl-4-cinnamate
1,2,2,6,6-Pentamethylpiperidinyl-4-diphenylacetate
1,2,2,6,6-Pentamethylpiperidinyl-4-n-dodecylthioacetate
1,2,2,6,6-Pentamethylpiperidinyl-4-(furan-2'-carboxylate)
1,2,2,6,6-Pentamethylpiperidinyl-dimethyl trimesate
1-n-Propyl-2,2,6,6-tetramethylpiperidinyl-acetate
1-n-Propyl-2,2,6,6-tetramethylpiperidinyl-4-octanoate
1-n-Propyl-2,2,6,6-tetramethylpiperidinyl-4-sterate
1-n-Octyl-2,2,6,6-tetramethylpiperidinyl-4-benzoate
1-n-Dodecyl-2,2,6,6-tetramethylpiperidinyl-4-n-octanoate
1-n-Dodecyl-2,2,6,6-tetramethylpiperidinyl-4-p-chlorobenzoate
1-n-Octadecyl-2,2,6,6-tetramethylpiperidinyl-4-benzoate
1-Allyl-2,2,6,6-tetramethylpiperidinyl-4-n-octanoate
1-Allyl-2,2,6,6-tetramethylpiperidinyl-4-cyclohexanecarboxylate
1-Allyl-2,2,6,6-tetramethylpiperidinyl-4-benzoate
1-α-Methallyl-2,2,6,6-tetramethylpiperidinyl-4-acetate
1-Oleyl-2,2,6,6-tetramethylpiperidinyl-4-cyclohexanecarboxylate
1-Propargyl-2,2,6,6-tetramethylpiperidinyl-4-p-methoxybenzoate
1-Benzyl-2,2,6,6-tetramethylpiperidinyl-4-n-octanoate
1-Benzyl-2,2,6,6-tetramethylpiperidinyl-4-(2'-ethylhexanoate)
1-Benzyl-2,2,6,6-tetramethylpiperidinyl-4stearate
1-Benzyl-2,2,6,6-tetramethylpiperidinol-4-benzoate
1-(2'-Hydroxyethyl)-2,2,6,6-tetramethylpiperidinyl-4-acetate
1-(2'-Hydroxyethyl)-2,2,6,6-tetramethylpiperidinyl-4-laurate
1-(2'-Hydroxyethyl)-2,2,6,6-tetramethylpiperidinyl-4-stearate
1-(2'-Hydroxyethyl)-2,2,6,6-tetramethylpiperidinyl-4-benzoate
1-(2'-Hydroxypropyl)-2,2,6,6-tetramethylpiperidinyl-4-oleate
1-(2'-Hydroxy-2'-phenylethyl)-2,2,6,6-tetramethylpiperidinyl-4-phenylacetate
1-(2'-Chloroethyl)-2,2,6,6-tetramethylpiperidinyl-4-n-octanoate
1-(2'-Bromopropyl)-2,2,6,6-tetramethylpiperidinyl-4-cyclohexane-carboxylate
1-(2'-Chloro-2'-phenylethyl)-2,2,6,6-tetramethylpiperidinyl-4-p-methoxybenzoate
1-(2' -Cyanoethyl)-2,2,6,6-tetramethylpiperidinyl-4-benzoate
1-(2'-.[.cycanopropyl).]..Iadd.Cyanopropyl.Iaddend.-2,2,6,6-tetramethylpiperidinyl-4-p-chlorobenzoate
1-(2',3'-.[.epoxypropyl).]..Iadd.Epoxypropyl).Iaddend.-2,2,6,6-tetramethylpiperidinyl-4-acetate
1-(2'-.[.ethoxypropyl).]..Iadd.Ethoxypropyl).Iaddend.-2,2,6,6-tetramethylpiperidinyl-4-(2'-ethylhexanoate)
1-(2'-.[.ethoxy).Iadd.Ethoxy.Iaddend.-2'-phenylethyl)-2,2,6,6-tetramethylpiperidinyl-4-diphenylacetate
1-(2'-.[.acetoxyethyl).]..Iadd.Acetoxyethyl).Iaddend.-2,2,6,6-tetramethylpiperidinyl-4-laurate
1-[2'-.[.(methylcarbamoyloxy).]..Iadd.(Methylcarbamoyloxy).Iaddend.ethyl]-2,2,6,6-tetramethylpiperidinyl-4-benzoate
1-[2'-.[.(phenylcarbamoyloxy).]..Iadd.(Phenylcarbamoyloxy).Iaddend.ethyl]-2,2,6,6-tetramethylpiperidinyl-4-isobutyrate
1-[2'-.[.(ethylthiocrbamoyloxy).]..Iadd.(Ethylthiocarbamoyloxy).Iaddend.ethyl]-2,2,6,6-tetramethylpiperidnyl-4-pivalate
1-Methylcarbonylmethyl-2,2,6,6-tetramethylpiperidinyl-4-phenylacetate
1-[2'-.[.(methylcarbonyl).]..Iadd.(Methylcarbonyl).Iaddend.ethyl]-2,2,6,6-tetramethylpiperidinyl-4-acetate
1-Ethoxycarbonylmethyl-2,2,6,6-tetramethylpiperidinyl-4-p-methoxybenzoate
1-[2'-(Methoxycarbonyl)ethyl]-2,2,6,6-tetramethylpiperidinyl-4-p-toluate
1-Carbamoylmethyl-2,2,6,6-tetramethylpiperidinyl-4-p-methoxybenzoate
1-(2'-Carbamoylethyl)-2,2,6,6-tetramethylpiperidinyl-4-stearate
1-[2'-.[.(methylcarbamoyl).]..Iadd.(Methylcarbamoyl).Iaddend.ethyl]-2,2,6,6-tetramethylpiperidinyl-4-octanoate
1-(Dimethylthiocarbamoyl)methyl-2,2,6,6-tetramethylpiperidinyl-4-isobutyrate
1-Acetyl-2,2,6,6-tetramethylpiperidinyl-4-acetate
1-Acetyl-2,2,6,6-tetramethylpiperidinyl-4-(2'-ethylhexanoate)
1-Acetyl-2,2,6,6-tetramethylpiperidinyl-4-stearate
1-Isobutyryl-2,2,6,6-tetramethylpiperidinyl-4-n-octanoate
1-Lauroyl-2,2,6,6-tetramethylpiperidinyl-4-eicosanoate
1-Stearoyl-2,2,6,6-tetramethylpiperidinyl-4-acetate
1-Benzoyl-2,2,6,6-tetramethylpiperidinyl-4-benzoate
1-Carbamoyl-2,2,6,6-tetramethylpiperidinyl-4-(1'-napthylacetate)
1-Methylcarbamoyl-2,2,6,6-tetramethylpiperidinyl-4-n-octanoate
1-Phenylcarbamoyl-2,2,6,6-tetramethylpiperidinyl-4-phenylacetate
1-Dimethylcarbamoyl-2,2,6,6-tetramethylpiperidinyl-4-laurate
1-Phenylthiocarbamoyl-2,2,6,6-tetramethylpiperidinyl-4p-t-butylbenzoate
4-.[.carbamoyloxy.]..Iadd.Carbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.methylcarbamoyloxy.]..Iadd.Methylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.dimethylcarbamoyloxy.]..Iadd.Dimethylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.isopropylcarbamoyloxy.]..Iadd.Isopropylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-t-.[.butylcarbamoyloxy.]..Iadd.Butylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-n-.[.hexylcarbamoyloxy.]..Iadd.Hexylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-[2'-.[.ethylhexylcarbamoyloxy].]..Iadd.Ethylhexylcarbamoyloxy].Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-n-.[.dodecylcarbamoyloxy.]..Iadd.Dodecylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-n-.[.octadecylcarbamoxyloxy.]..Iadd.Octadecylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.allylcarbamoyloxy.]..Iadd.Allylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.oleylcarbamoyloxy.]..Iadd.Oleylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.cyclohexylcarbamoyloxy.]..Iadd.Cyclohexylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-[3'-.[.methylcyclohexylcarbamoyloxy.]..Iadd.Methylcyclohexylcarbamoyloxy.Iaddend.]-1,2,2,6,6-pentamethylpiperidine
4-[4'-t-.[.butylcyclohexylcarbamoyloxy.]..Iadd.Butylcyclohexylcarbamoyloxy.Iaddend.]-1,2,2,6,6,-pentamethylpiperidine
4-.[.cyclohexylmethylcarbamoyloxy.]..Iadd.Cyclohexylmethylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperdine
4-.[.benzylcarbamoyloxy.]..Iadd.Benzylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.phenylcarbamoyloxy.]..Iadd.Phenylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.phenylthiocarbamoyloxy.]..Iadd.Phenylthiocarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-m-.[.tolylcarbamoyloxy.]..Iadd.Tolylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-p-.[.tolylcarbamoyloxy.]..Iadd.Tolycarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-p-.[.chlorophenylcarbamoyloxy.]..Iadd.Chlorophenylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-p-t-.[.butylphenylcarbamoyloxy.]..Iadd.Butylphenylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-α-.[.naphthylcarbamoyloxy.]..Iadd.Naphthylcarbamoyloxy.Iaddend.-1,2,2,6,6-pentamethylpiperidine
4-.[.cyclohexylcarbamoyloxy.]..Iadd.Cyclohexylcarbamoyloxy.Iaddend.-1-ethyl-2,2,6,6-tetramethylpiperidine
4-.[.methylcarbamoyloxy.]..Iadd.Methylcarbamoyloxy.Iaddend.-1-n-propyl-2,2,6,6-tetramethylpiperidine
4-.[.methylcarbamoyloxy.]..Iadd.Methylcarbamoyloxy.Iaddend.-1-secbutyl-2,2,6,6-tetramethylpiperidine
4-n-.[.octadecylcarbamoyloxy.]..Iadd.Octadecylcarbamoyloxy.Iaddend.-1-n-butyl-2,2,6,6-tetramethylpiperidine
4-Methylcarbamoyloxy-1-n-ocytyl-2,2,6,6-tetramethylpiperidine
4-methylcarbamoyloxy-1-n-octadecyl-2,2,6,6-tetramethylpiperidine
4-phenylcarbamoyloxy-1-allyl-2,2,6,6-tetramethylpiperidine
4-p-tolylcarbamoyloxy-1-oleyl-2,2,6,6-tetramethylpiperidine
4-methylcarbamoyloxy-1-propargyl-2,2,6,6-tetramethylpiperidine
4-phenylcarbamoyloxy-1-benzyl-2,2,6,6-tetramethylpiperidine
4-methylcarbamoyloxy-1-(2'-hydroxyethyl)-2,2,6,6-tetramethylpiperidine
4-cyclohexylcarbamoyloxy-1-(2'-chloropropyl)-2,2,6,6-tetramethylpiperidine
4-phenylcarbamoyloxy-1-(2'-hydroxy-2'-phenylethyl)-2,2,6,6-tetramethylpiperidine
4-methylcarbamoyloxy-1-(2',3'-epoxypropyl)-2,2,6,6-tetramethylpiperidine
4-carbamoyloxy-1-(2'-methoxyethyl)-2,2,6,6-tetramethylpiperidine
4-dimethylcarbamoyloxy-1-(2'-acetoxyethyl)-2,2,6,6-tetramethylpiperidine
4-n-hexylcarbamoyloxy-1-[2'-(methylcarbamoyloxy)ethyl-2,2,6,6-tetramethylpiperidine
4-methylcarbamoyloxy-1-methylcarbonylmethyl-2,2,6,6-tetramethylpiperidine
4-.[.phenylcarbamoyl.]..Iadd.phenylcarbamoyloxy.Iaddend.-1-(2'-methylcarbonylethyl)-2,2,6,6-tetramethylpiperidine
4-benzylcarbamoyloxy-1-carbamoylmethyl-2,2,6,6-tetramethylpiperidine
4-n-dodecylcarbamoyloxy-1-(2'-carbamoylethyl)-2,2,6,6-tetramethylpiperidine
4-methylcarbamoyloxy-1-(2'-thiocarbamoylethyl)-2,2,6,6-tetramethylpiperidine
4-methylcrbamoyloxy--phenylcarbamoyloxy-acetyl-2,2,6,6-tetramethylpiperidine
4-phenylcarbamoyloxy-1-stearoyl-2,2,6,6-tetramethylpiperidine
4-methylthiocarbamoyloxy-1-lauroyl-2,2,6,6-tetramethylpiperidine
4-[2'-ethylhexylcarbamoyl]-1-benzoyl-2,2,6,6-tetramethylpiperidine
4-carbamoyloxy-1-carbamoyl-2,2,6,6-tetramethylpiperidine
4-methylcarbamoyloxy-1-methylcarbamoyl-2,2,6,6-tetramethylpiperidine
4-phenylcarbamoyloxy-1-phenylcarbamoyl-2,2,6,6-tetramethylpiperidine
4-methylthiocarbamoyloxy-1-methylthiocarbamoyl-2,2,6,6-tetramethylpiperidine
4-phenythiocarbamoyloxy-1-phenylthiocarbamoyl-2,2,6,6-tetramethylpiperidine
4-dimethylcarbamoyloxy-1-dimethylcarbamoyl-2,2,6,6-tetramethylpiperidine
4-stearyloxy-1,2,2,4,6,6-hexamethylpiperidine
4-phenyl-1,2,2,6,6-pentamethyl-piperidinyl-4-n-octanoate
Examples where n=2
1,2-Bis(1',2',2',6',6'-pentamethyl-4'-piperidyloxy)ethane
1,4-Bis(1'-n-propyl-2',2',6',6'-tetramethyl-4'-piperidyloxy) butene
1,6-Bis(1'-n-octadecyl-2',2',6',6'-tetramethyl-4'-piperdinyloxy)hexane
1,4-Bis(1'-allyl-2',2',6',6'-tetramethyl-4'-piperidyloxy) cyclohexane
1,4-Bis(1'-propargyl-2',2',6',6'-tetramethyl-4-piperidyloxy) but-2-ene
α,α-Bis(1-benzyl-2,2,6,6-tetramethyl-4-piperidyloxy)p-xylene
1,3-Bis[1'-(2"-hydroxyethyl)-2',2',6',6'-tetramethyl-4'-piperidyloxy]benzene
1,2-Bis[1'-(2"-cyanoethyl)-2',2',6',6'-tetramethyl-4'-piperidyloxy]ethane
1,4-Bis(1'-acetyl-2',2',6',6'-tetramethyl-4'-piperidyloxy) but-2-yne
4,4-Bis(1"-methylcarbamoyl-2",2",6",6"-tetramethyl-4"-piperidyloxy)diphenylmethane
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)carbonate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)oxalate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)malonate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)adipate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)sebacate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)fumarate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)isophthalate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)cyclohexane 1',4'-dicarboxylate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)thiodipropionate
Bis(1,2,2,6,6-pentamethyl-4-piperidinyl)methyltrimesate
Bis(1-n-propyl-2,2,6,6-tetramethyl-4-piperidinyl)adipate
Bis(1-secbutyl-2,2,6,6-tetramethyl-4-piperidinyl)succinate
Bis(1-n-octyl-2,2,6,6-tetramethyl-4-piperidinyl)sebacate
Bis(1-n-dodecyl-2,2,6,6-tetramethyl-4-piperidinyl)adipate
Bis(1-n-octadecyl-2,2,6,6-tetramethyl-4-piperidinyl)sebacate
Bis(1-allyl-2,2,6,6-tetramethyl-4-piperidinyl)adipate
Bis(1-allyl-2,2,6,6-tetramethyl-4-piperidinyl)thiophene-2',5'-dicarboxylate
Bis(1-oleyl-2,2,6,6-tetramethyl-4-piperidinyl)thiodipropionate
Bis(1-propargyl-2,2,6,6-tetramethyl-4-piperidinyl)sebacate
Bis(1-benzyl-2,2,6,6-tetramethyl-4-piperdinyl(sebacate
Bis[1-(2'-hydroxyethyl)-2,2,6,6-tetramethyl-4-piperidinyl]adipate
Bis[1-(2'-chloropropyl)-2,2,6,6-tetramethyl-4-piperidinyl]succinate
Bis[1-(2'-cyanoethyl)-2,2,6,6-tetramethyl-4-piperidinyl]sebacate
Bis[1-(2',3'-epoxypropyl)-2,2,6,6-tetramethyl-4-piperidinyl]azelate
Bis[1-(2'-methoxyethyl)-2,2,6,6-tetramethyl-4-piperidinyl] pimelate
Bis[1-(2'-acetoxyethyl)-2,2,6,6-tetramethyl-4-piperidinyl] glutarate
Bis[1-(2'-methylcarbamoyloxyethyl)-2,2,6,6-tetramethyl-4-piperidinyl]malonate
Bis[1-(methylcarbonylmethyl)-2,2,6,6-tetramethyl-4-piperidinyl]terephthalate
Bis[1-carbamoylmethyl-2,2,6,6-tetramethyl-4-piperidinyl] cyclohexane-1',4'-dicarboxylate
Bis[1-(methylcarbamoylethyl)-2,2,6,6-tetramethyl-4-piperidinyl]thiodipropionate
Bis[1-acetyl-2,2,6,6-tetramethyl-4-piperidinyl]sebacate
Bis[1-stearoyl-2,2,6,6-tetramethyl-4-piperidinyl]succinate
Bis[1-Benzoyl-2,2,6,6-tetramethyl-4-piperidinyl]dodecandioate
Bis[1-methylcarbamoyl-2,2,6,6-tetramethylpiperidinyl]adipate
Bis[1-phenylthiocarbamoyl-2,2,6,6-tetramethylpiperidinyl]isophthalate
.[.ethane.]. .Iadd.Ethane.Iaddend.-1',2'-bis[1,2,2,6,6-pentamethylpiperidine]
.[.hexane.]. .Iadd.Hexane.Iaddend.-1',6'-bis[4-carbamoyloxy-1,2,2,6,6-pentamethylpiperidine]
2',4',4'.[.-trimethylhexane.]. .Iadd.- Trimethylhexane.Iaddend.-1',6'-bis[4-carbamoyloxy-1,2,2,6,6-pentamethylpiperidine]
.[.cyclohexane.]. .Iadd.Cyclohexane.Iaddend.-1',3'-bis[4-carbamoyloxy-1,2,2,6,6-pentamethylpiperidine]
.[.benzene.]. .Iadd.Benzene.Iaddend.-1',4'-bis[4-carbamoyloxy-1,2,2,6,6-pentamethylpiperidine]
.[.toluene.]. .Iadd.Toluene.Iaddend.-2',4'-bis[4-thiocarbamoyloxy-1,2,2,6,6-pentamethylpiperidine]
.[.toluene.]. .Iadd.Toluene.Iaddend.-2',4'-bis[4-thiocarbamoyloxy-1,2,2,6,6-pentamethylpiperidine]
.[.naphthalene.]. .Iadd.Naphthalene.Iaddend.-1',5'-bis[4-carbamoyloxy-1,2,2,6,6-pentamethylpiperidine]
.[.diphenylmethane.]. .Iadd.Diphenylmethane.Iaddend.-4',4"-bis[4-carbamoyloxy-1,2,2,6,6-pentamethylpiperidine]
.[.toluene.]. .Iadd.Toluene.Iaddend.-2',4'-bis[4carbamoyloxy-1-n-propyl-2,2,6,6-tetramethylpiperidine]
.[.hexane.]. .Iadd.Hexane.Iaddend.-1',6'-bis[4-carbamoyloxy-1-n-butyl-2,2,6,6-tetramethylpiperidine]
Hexane-1',6'-bis[4-carbamoyloxy-1-n-octyl-2,2,6,6,2',4',4'-trimethylhexane-1',6'-bis[4-carbamoyloxy-1-n-octadecyl-2,2,6,6-tetramethylpiperidine]
Cyclohexane-1',4'-bis[4-carbamoyloxy-1-allyl-2,2,6,6-tetramethylpiperidine]
2',4',4'-trimethylhexane-1',6'-bis[4-carbamoyloxy-1-allyl-2,2,6,6-tetramethylpiperidine]
Benzene-1',4'-bis[4-carbamoyloxy-1-propargyl-2,2,6,6-tetramethylpiperidine]
toluene-2',4'-bis[4-carbamoyloxy-1-benzyl-2,2,6,6-tetramethylpiperidine]
Toluene-2",4<-bis[4-carbamoyloxy-1-(2'-hydrocyethyl)-2,2,6,6-tetramethylpiperidine].[.Diphenylmethane.].-4',4"-bis.Iadd.Diphenylmethane-[4-carbamoyloxy-1-(2'-cyanoethyl)-2,2,6,6-tetramethylpiperidine]
Toluene-2",4"-bis[4-carbamoyloxy-1-(2"-acetoxyethyl)-2,2,6,6-tetramethylpiperidine]
Ethane-1',2'-bis[4-carbamoyloxy-1-methylcarbonylmethyl-2,2,6,6-tetramethylpiperidine]
Hexane-1",6"-bis[4-carbamoyloxy-1-(2'-methylcarbamoylethyl)-2,2,6,6-tetramethylpiperidine]
Naphthalene-1',5'-bis[4-carbamoyloxy-1-acetyl-2,2,6,6-tetramethylpiperidine]
2.40, 4',4'-trimethylhexane-1',6'-[4-carbamoyloxy-1-stearoyl-2,2,6,6-tetramethylpiperidine]
Hexane-1',6'-bis[4-carbamoyloxy-1-methylcarbamoyl-2,2,6,6-tetramethylpiperidine]
Bis[1,2,2,6,6-pentamethyl-4-piperidinyl]ether
Examples where n=3
Tris(1,2,2,6,6-pentamethyl-4-piperidinyl)nitrilotriacetate
Tris(1,2,2,6,6-pentamethyl-4-piperidinyl)tricarballylate
Tris(1,2,2,6,6,4"4-piperidinyl)trimesate
Diphenylmethane-
Tris(1,2,2,6,6-pentamethyl-4-piperidinyl)trimellitate
Tris(1,2,2,6,6-pentamethyl-4-piperidinyl)phosphite
Tris(1,2,2,6,6-pentamethyl-4-piperidinyl)phosphate
Tris(1,2,2,6,6-pentamethyl-4-piperidinyl)borate
Tris(1-n-octadecyl-2,2,6,6-tetramethyl-4-piperidinyl)-trimesate
Tris(1-allyl-2,2,6,6-tetramethyl-4-piperidinyl)phosphite
Tris(1-propargyl-2,2,6,6-tetramethyl-4-piperidinyl)borate
Tris(1-benzyl-2,2,6,6-tetramethyl-4-piperidinyl)trimellitate
Tris[1-(2'-hydroxyethyl)-2,2,6,6-tetramethyl-4-piperidinyl]trimesate
Tris[1-(2'-cyanoethyl)-2,2,6,6-tetramethyl-4- piperidinyl]phosphite
Tris[1-acetyl-2,2,6,6-tetramethyl-4-piperidinyl)borate
Tris[1-methylcarbamoyl-2,2,6,6-tetramethyl-4-piperidinyl]trimesate
Examples where n=4
Tetrakis(1,2,2,6,6-pentamethyl-4-piperidinyl)ethylenediamine tetracarboxylate
Tetrakis(1,2,2,6,6-pentamethyl-4-piperidinyl)pyromellitate
Tetrakis(1,2,2,6,6-pentamethyl-4-piperidinyl)o-silicate
Tetrakis(1-n-octyl-2,2,6,6-tetramethyl-4-piperidinyl)pyromellitate
Tetrakis(1-allyl-2,2,6,6-tetramethyl-4-piperidinylpyromellitate Tetrakis(1-propargyl-2,2,6,6-tetramethyl-4-piperidinyl)-o-silicate
Tetrakis(1-benzyl-2,2,6,6-tetraethyl-4-piperidinyl)ethylenediamine tetracarboxylate
Tetrakis[1-(2'-hydroxypropyl)-2,2,6,6-tetramethyl-4-piperidinyl]-o-silicate
Tetrakis[1-stearoyl-2,2,6,6-tetramethyl-4-piperidinyl]pyromellitate
Tetrakis[1-phenylcarbamoyl-2,2,6,6-tetramethyl-4-piperidinyl]-o-silicate
The invention also includes salts of the compounds of Formula I, for instance salts of inorganic acids such as phosphates, carbonates, sulphates and chlorides and salts of organic acids such as acetates, stearates, maleates, citrates, tartrates, oxalates, benzoates and substituted carbamic acids.
Examples of salts are
4-n-butoxy-1,2,2,6,6-pentamethylpiperidine dihydrogen phosphate
4-n-dodecyloxy-1,2,2,6,6-pentamethylpiperidine hydrochloride bis(1,2,2,6,6-pentamethyl-4-piperidinyl)sebacate sulphate
1,2,2,6,6-pentamethylpiperidinyl-4-beta-(3',5'-di-t-butyl-4'-hydroxyphenyl)propionate.bicarbonate
4-methylcarbamoyloxy-1,2,2,6,6-pentamethylpiperidine.acetate
1,6-bis(4'-carbamoyloxy-1',2',2',6',6'-pentamethylpiperidine hexane stearate
4-phenyl carbamoyloxy-1,2,2,6,6-pentamethylpiperidine.benzoate
1,2,2,6,6-pentamethylpiperidinyl-4-n-octanoate 3',5'-di-t-butyl-4'-hydroxybenzoate
1,4-bis(1',2',2',6',6'-pentamethyl-4'-piperidyloxy)butane hydrogen oxalate
4-(2'-cyanoethyoxy)1,2,2,6,6-pentamethylpiperidine hydrogen maleate
4-stearylcarbamoyloxy-1,2,2,6,6-pentamethylpiperidine.citrate
1-(2'-hydroxyethyl)-2,2,6,6-tetramethylpiperidinyl-4-n-octanoate.tartrate
1,2,2,6,6-pentamethylpiperidinyl-4-benzoate.dibutyl carbamate.
R1 or R3 can be represented by a monovalent, divalent or trivalent group obtained by removing 1 to 3 hydroxyl groups from a sulphonic acid, a sulphinic acid, a disulphonic acid, a phosphorus containing acid, such as o-phosphoric or o-phosphorous acid or a boric acid. The following list shows compounds with acid radicals for R3. However, the same radicals are also examples for R1.
a. when n is 1
1,2,2,6,6-pentamethylpiperidinyl-4-benzene sulphinate
1,2,2,6,6-pentamethylpiperidinyl-4-benzene sulphonate
1,2,2,6,6-pentamethylpiperidinyl-4-methyl sulphate
1,2,2,6,6-petamethylpiperidinyl-4-dimethylborate
1,2,2,6,6-petamethylpiperidinyl-4-phenyl phosphonate
1,2,2,6,6-pentamethylpiperidinyl-4-dimethyl phosphite
1,2,2,6,6-pentamethykpiperidinyl-4-diphenyl phosphate
b. when n is 2
bis(1,2,2,6,6-pentamethyl-4-piperidinyl)sulphate
bis(1,2,2,6,6-pentamethyl-4-piperidinyl)phosphonate
bis(1,2,2,6,6-pentamethyl-4-piperidinyl)phenyl phosphate
bis(1,2,2,6,6-pentamethyl-4-piperidinyl)benzene-1,3-disulphinate
c. when n is 3
tris(1,2,2,6,6-pentamethyl-4-piperidinyl)-benzene-1,3,5-trisulphonate
tris(1,2,2,6,6-pentamethyl-4-piperidinyl)-benzene-1,3,5-trisulphinate.
A preferred sub-group of compounds of formula 1 are those compounds having the formula: ##STR14## and their salts, wherein Y is an alkyl group having from 1 to 20, preferably 1 to 4, carbon atoms, alkenyl having from 3 to 20 carbon atoms or an aralkyl residue, preferably having from 7 to 9 carbon atoms, and n1 is 1 or 2; when n1 is 1, R is hydrogen or a monovalent aliphatic residue having from 1 to 20, preferably 6 to 20 carbon atoms, a monovalent alicyclic residue having from 5 to 12 carbon atoms, or a monovalent aromatic residue having from 6 to 20 carbon atoms; or ##STR15## and when n1 is 2, R is a divalent aliphatic residue having from 1 to 20, preferably 4 to 20 carbon atoms, a divalent alicyclic residue having from 5 to 12 carbon atoms or a divalent aromatic residue having from 6 to 14 carbon atoms. Two sub-groups of the compounds of the formula Ia are those having as Y alkyl from 1 to 4 carbon atoms and alkyl having 5 to 20 carbon atoms.
Examples of substituents Y are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.butyl, n-hexyl, n-octyl, n-dodecyl, n-octadecyl, eicosyl, allyl, methallyl, oleyl, benzyl, α-methylbenzyl, p-methylbenzyl and p-methyl-α-methylbenzyl, However, it is particularly preferred that Y is methyl.
When n1 is 1, R can be hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.butyl, t-butyl, n-pentyl, 1-ethylpropyl, 2-methylbutyl, n-hexyl, 2-methylpentyl, n-heptyl, 2-ethylpentyl, n-octyl, 2,2,4-trimethylpentyl, n-decl, n-undecyl, n-tridecyl, n-pentadecyl, n-heptadecyl, eicosyl, vinyl α- or β-methylvinyl, dec-9-enyl, heptadec-8-enyl, β-methythioethyl, β-octylthioethyl, β-dodecylthioethyl, cyclopentyl, cyclohexyl, cyclohex-3-enyl, methylcyclohexyl, t-butylcylohexyl, cyclododecyl, 1- or 2-perhydronaphthyl, adamantyl, cyclopentylmethyl, cyclohexylmethyl, β-cyclohexylethyl, 1- or 2-(perhydronaphthyl)methyl, β-1- or 2-perhydronaphthyl[ethyl, benzyl, β-phenylethyl, β-phenylvinyl, 1- or 2-naphthylmethyl, β-[1- or 2-naphthyl]ethyl, phenyl, o-, m- or p-tolyl, o-, m- or p-ethylphenyl, o-, m- or p-isopropylphenyl, o-, m- or p-t-butylphenyl, phenylphenyl, 4-methyl.1-naphthyl, 4-ethyl-1-naphthyl, 4-isopropyl-1-naphthyl or 4-t-butyl-1-naphthyl or the group ##STR16##
Particularly preferred substituent groups R are those listed above containing from 6 to 20 carbon atoms, as well as the group having the formula: ##STR17## wherein R10 and R11 are the same or different and each is an alkyl group having from 1 to 6, preferably 1 to 4 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, sec.butyl, t-butyl, t-pentyl, (1,1,-dimethylpropyl), t-hexyl (1,1,-dimethylbutyl), but preferably methyl, isopropyl or t-butyl groups: A is -CH2-, ##STR18## and p is 0 or 1.
When n1 is 2, R can be methylene, 1,2,-ethylene, 1,4-n-butylene, 1,8-n-octylene, 2,2,4-trimethyl-1, 4-butylene, 1,10-n-decylene, 1,2-eicosylene, vinylene, propenylene, 1,2-, 1,3- and 1,4-cyclohexylene, cyclohexyl-3-ene, 11,2-, 1,3- and 1,4-phenylene, p-xylylene, 1,4-, and 1,5-naphthylene, diphenylene or diphenylmethylene.
Specific examples of compounds having the formula Ia are shown on the preceding pages .[.to.]..
A further preferred sub-group of compounds of formula I are those having the formula: ##STR19## and is salts wherein Y1 is an alkyl residue having from 1 to 12 carbon atoms, an alkenyl residue having from 3 to 12 carbon atoms or an aralkyl residue having from 7 to 9 carbon atoms and R12 is hydrogen or an alkyl or alkylen containing up to 20 carbon atoms, and substituted alkyl having the formula ##STR20## wherein m is 1, 2 or 3, R4 is hydrogen or methyl, .[.S1.]. X1 is halogen or methoxy and X2 is halogen or R12 is an alkenyl or alkenylen having up to .Badd.20 carbon atoms, a cycloalkyl or cycloalkyliden having 5 to 12 carbon atoms, an aryl or arylen having 6 to 12 carbon atoms and q is 1 or 2.
Two sub-groups of compounds of the formula Ib are those having as Y1 alkyl from 1 to 4 and alkyl having 5 to 12 carbom atoms.
When q is 1, R12 can be for example hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, secbutyl, t-butyl, n-pentyl, 2-ethylpropyl, 2-methylbutyl, n-hexyl, 2-methylpentyl, n-heptyl, 2-ethylpentyl, n-octyl, 2-ethylhexyl, 2,2,4-trimethylpentyl, n-decyl, n-dodecyl, n-tetradecyl, n-octadecyl, eicosyl, mesityl, allyl, oleyl, cyclopentyl, cyclohexyl, methylcyclohexyl, t-butylcyclohexyl, t-octylcylohexyl, cyclododecyl, 1- and 2-perhydronaphthyl, adamantyl, cyclopentylmethyl, cyclohexylmethyl, β-cyclohexylethyl, benzyl, .[.β-Phenylethyl.]. .Iadd.β-phenylethyl.Iaddend., 1- and 2-naphthylmethyl, β[1- and 2-naphthyl]ethyl, phenyl, o-, m- and and p-tolyl, 2,4- and 2,6-xylyl, phenyl, o-, m-and p-tolyl, 2,4- and 2,6-xylyl, p-chlorophenyl, 3-chloro-p-tolyl, o-ethylphenyl, p-t-butylphenyl, 2,3- and 2,5-di-chlorophenyl, α- and β- naphthyl, phenylphenyl. Preferred monovalent groups R12 are hydrocarbyl groups such as methyl, ethyl, propyl, isopropyl, n-butyl, 2-ethylhexyl, dodecyl, octadecyl, allyl, oleyl, cyclohexyl, benzyl, phenyl, o-, m- and p-tolyl, 2,4- and 2,6-xylyl and naphthyl.
When q is 2, R12 can be for example methylene, 1,2-ethylene, 1,4-n-butylene, 1,6-n-hexylene, 1,8-n-octylene, 2,4,4-trimethyl-1,6-hexylene, 1,10-n-decylene, 1,2-eicosylene, 1,2-eicosenylene, 1,3- and 1,4-cyclohexylene, 1,3- and 1,4-phenylene, 2,4-tolylene, 1,5-naphthylene, 4,4'-diphenylene, 4'-diphenylemethylene, 3,3'-dimethyl-4,4'-diphenylene, 3,3'-dimethyl-4,4'-diphenylmethylene.
Preferred divalent groups R12 are 1,2-ethylene, 1,6-hexylene, 2,4,4-trimethyl-1,6-hexylene, 1,3- and 1,4-phenylene, 2,4-tolylene, 1,5-naphthylene, 4,4'-diphenylmethylene.
In the above formula Ib, examples of the group Y1 are methyl, ethyl, n-propyl, isopropyl, n-butyl, secbutyl, n-hexyl, n-octyl, n-dodecyl, allyl, α-methallyl, 10-undecenyl, benzyl, α-methylbenzyl, p-methylbenzyl, p-methyl-α-methylbenzyl, α-naphthylmethyl. Particularly preferred are straight or branched alkyl having 1 to 4 carbon atoms and for reasons of ease of preparation the most preferred meaning for Y1 is methyl.
Specific examples of the carbamoyloxy derivatives of N-substituted-2,2,6,6-tetrasubstituted piperidin-4-ols of formula .[.Ie.]. .Iadd.Ib .Iaddend.are given in the preceding pages .[.19 and 20..]..Iadd.. .Iaddend.
The following groups A to O are subgroups of compounds of the formula I.
A. Compounds of formula I wherein when n is 1, R3 is a monovalent residue and is an alkyl residue having from 1 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an alkenyl or alkynyl residue having from 3 to 20 carbom atoms, an aralkyl residue having from 7 to 12 carbon atoms, or a residue having the formula: ##STR21## wherein m is 1, 2 or 3, R4 is a hydrogen, methyl or phenyl residue, X2 is halogen, cyano, ##STR22## --COR5, --CO.OR5, --CO.SR5 or --CONR5 R6 and X1 is hydroxyl, halogen, cyano, -OR5, ##STR23## wherein R5 is an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 2 to 20 carbon atoms, a cycloalkyl residue having 5 to 12 carbon atoms, an aryl residue having from 6 to 11 carbon atoms or an aralkyl residue having 7 to 14 carbon atoms or when R5 is joined to a nitrogen atom, also hydrogen and R6 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, or R5 and R6 together with the nitrogen atom to which they are bound form a 5- or 6-membered ring which contains no other heteroatoms or contains one or more other heteroatoms or R3 is an aryl residue or a residue having the formula: ##STR24## wherein R1 ' is hydrogen or R1 ' has the same significance as R1 of formula I; when n is 2, R3 is a divalent residue and is an alkylene residue having from 1 to 20 carbon atoms, an alkenylene residue having from 2 to 20 carbon atoms, an alkynylene residue having from 2 to 20 carbon atoms, a cycloalkyliden residue having from 3 to 12 carbon atoms, an arylene residue having 6 to 14 carbon atoms; when n is 3, R3 is a trivalent residue and is an alkanetriyl, an arenetriyl or an arenetriyltrialkylene residue, and when n is 4, R3 is a tetravalent residue and is an alkanetetrayl residue.
B. Compounds of the formula I wherein when n is I R3 is an acyl group ##STR25## wherein R7 is hydrogen, an unsubstituted aliphatic or substituted aliphatic residue having from 1 to 20 carbon atoms, an alkenyl or alkynyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, an aromatic residue having from 6 to 20 carbon atoms, or an heterocyclic residue, or R3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid, when n is 2,R3 is an divalent residue of an aliphatic, aromatic or heterocyclic diacyl, the group --CO-- or --CO.CO--, a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or a boric acid; when n is 3,R3 is a trivalent residue of an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric, o-phosphorous or o-boric acid; and when n is 4,R3 is a tetravalent residue of a tetraacyl residue derived from an aliphatic or aromatic tetracarboxylic acid or from o-silicic acid.
C. Compounds of the formula I wherein n is 1 or 2 and when n is 1 R3 is a carbamoyl residue having the formula: ##STR26## wherein R8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, and R9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an unsubstituted aryl or substituted aryl residue having from 6 to 12 carbon atoms; and when n is 2 R3 is a divalent aliphatic or aromatic dicarbamoyl residue.
D. Compounds of the formula I wherein n is 1 or 2 and when n is 1 R3 is a thiocarbamoyl residue having the formula: ##STR27## wherein R8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, and R9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an unsubstituted aryl or substituted aryl residue having from 6 to 12 carbon atoms; and when n is 2,R3 is a divalent aliphatic or aromatic dithiocarbamoyl.
E. Compounds of the formula I wherein when n is 1 R3 is a monovalent residue and is an alkyl residue having from 1 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an alkenyl or alkynyl residue having from 3 to 20 carbon atoms, an aralkyl residue having from 7 to 9 carbon atoms, or a residue having the formula: ##STR28## wherein m is 1, 2 or 3, R4 is a hydrogen, methyl or phenyl residue, X2 is halogen, cyano, ##STR29## --COR5, --CO.OR5, --CO.SR5 or --CONR5 R6 and X1 is hydroxyl, halogen, cyano, --OR5, --O--CO.R5, --OCSR5, --O.CO.NR5 R6,--CO.R5, --CO.OR5, --CO.SR5, --CO.NR5 R6 or --CS.NR5 R6, wherein R5 is an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 2 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbom atoms, an aryl residue having from 6 to 11 carbon atoms, or an aralkyl residue having 7 to 11 carbon atoms, or when R5 is joined to a nitrogen atom, also hydrogen and R6 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, or R5 and R6 together with the nitrogen atom to which they are bound form a 5- or 6-membered ring which contains no other heteroatoms or contains one or more other heteroatoms or R3 is an aryl residue or a residue having the formula: ##STR30## wherein R1 ' is hydrogen or R1 ' has the same significance as R1 of claim 2; when n is 2, R3 is a divalent residue and is an alkylene residue having from 1 to 20 carbon atoms, an alkenylene residue having from 3 to 20 carbon atoms, an alkynylene residue having from 3 to 20 carbon atoms, an arylene residue having 6 to 14 carbon atoms, an aralkylene residue having from 8 to 14 carbon atoms; when n is 3, R3 is a trivalent residue of an alkanotriyl, an arenetriyl, or arenetriyltrialkylene group; and when n is 4, R3 is tetravalent residue of an alkanetetrayl group.
F. Compounds of the formula I wherein when n is 1 R3 is an acyl group ##STR31## wherein R7 is an aliphatic or substituted aliphatic residue having from 1 to 20 carbon atoms, an alkenyl or alkynyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, an aromatic residue having from 6 to 12 carbon atoms or an heterocyclic residue, with the proviso that only one of R1 and R3 can represent an unsaturated acyl group or R3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid, when n is 2, R3 is a divalent residue of an aliphatic, aromatic or heterocyclic diacyl residue, a carbonyl, sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or a boric acid; when n is 3, R3 is a trivalent residue of an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric, o-phosphorous or o-boric acid and when n is 4, R3 is a tetravalent residue of a tetraacyl residue derived from an aliphatic or aromatic tetracarboxylic acid or from o-silicic acid.
.[.G. Compound of the formula I wherein n is 1 or 2 and when n is 1, R3 is a carbamoyl residue having the formula: .]. ##STR32## .[.wherein R8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, and R9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an aryl or substituted aryl residue having from 6 to 12 carbon atoms; and when n is 2, R3 is a divalent residue of an aliphatic or aromatic dicarbamoyl residue..].
.[.H. Compounds of the formula wherein n is 1 or 2 and when n is 1, R3 is a thiocarbamoyl residue having the formula: .]. ##STR33## .[.wherein R8 is hydrogen or an alkyl residue having from 1 to 4 carbon atoms, and R9 is hydrogen, an alkyl residue having from 1 to 20 carbon atoms, an alkenyl residue having from 3 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms or an aryl or substituted aryl residue having from 6 to 12 carbon atoms; and when n is 2, R3 is a divalent residue of an aliphatic or aromatic dithiocarbamoyl residue..].
.[.I..]. .Iadd.G. .Iaddend.Compounds of formula I and their bicarbonate wherein n is 1, 2 or 3 R1 is alkyl having from 1 to 18 carbon atoms, benzyl or alkenyl having 3 carbon atoms or a group of the formula: ##STR34## wherein R4 is hydrogen, methyl or phenyl and X1 is a group of the formula ##STR35## and X2 is a group of the formula ##STR36## wherein .[.R3.]. R5 is alkyl having .Badd.1 or 2carbon atoms or phenyl or R1 is a group of the formula and R2 is hydrogen and R3 when n is 1 is alkyl having 3 to 18 carbon atoms, alkenyl having 3 carbon atoms, propargyl, benzyl, .[.--CH2 CH2 CH.]. .Iadd.CH2 CH2 CN .Iaddend.or a group of the formula
--CH.sub.2 X.sub.2
wherein X2 is ##STR37## .[.of.]. .Iadd.or is a group .Iaddend.of the formula ##STR38## wherein R7 is alkyl having 1 to 19 carbon atoms, CH3 (CH2)11 --S--CH2 --, cycloalkyl having 6 to 10 carbon atoms, alkenyl having 2 to 17 carbon atoms, unsubstituted aralkyl having 7 to 13 carbon atoms, C6 H5 -CH═CH--, aralkyl substituted by hydroxy or butyl, unsubstituted aryl having 6 to 10 carbon atoms, aryl substituted by alkyl having 1 to 4 carbon atoms, CH3 O--, Cl, OH or ##STR39## or of the formula ##STR40## wherein R9 is alkyl having 1 to 8carbon atoms, alkenyl having 3 carbon atoms, cyclohexyl, unsubstituted aryl having 6 to 10 carbon atoms, aryl substituted by methyl or Cl or R3 when n is 2 is the group --CO--R--CO-- wherein R is alkylen having 4 to 8 carbon atoms, --CH2 CH2 --S--CH2 CH2 --, vinylen, cyclohexylen, a divalent thiophen residue, unsubstituted .[.phenylen.]. .Iadd.phenylene .Iaddend.or .[.phenylen.]. .Iadd.phenylene .Iaddend.substituted by ##STR41## or a group of the formula --CONHR1 NHCO-- wherein R1 is hexylen, unsbustituted arylene having 6 to 10 carbon atoms, arylene substituted by methyl or R1 is the group ##STR42## or a group of the formula --COCO-- or butylen or R3 when n is 3, is ##STR43##
.[.J..]. .Iadd.H. .Iaddend.Compounds of the formula I wherein n is 1, 2 or 4 and when n is 1, R3 is an acyl group ##STR44## wherein R7 is hydrogen, an substituted aliphatic residue having from 1 to 20 carbon atoms, a alkenyl or alkynyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, or an heterocyclic residue, or R3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid, or when n is 2, R3 is an divalent residue of heterocyclic diacyl residue or a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or a boric acid; or when n is 4, R3 is a tetraacyl residue derived from an aliphatic tetracarboxylic acid.
.[.K..]. .Iadd.I. .Iaddend.Compounds of the formula I wherein n is 1, 2 and 4 and when n is 1, R3 is an acyl group ##STR45## wherein R7 is hydrogen, a cycloliphatic residue having from 5 to 12 carbon atoms or a heterocyclic residue or R3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid or when n is 2, R3 is a divalent residue of a heterocyclic diacyl or a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or when n is 4, R3 is a tetraacyl residue derived from an aliphatic tetracarboxylic acid.
.[.L. Compounds of the formula I wherein n is 1, 2 or 4 and when n is 1, R3 is an acyl group .]. ##STR46## .[.wherein R7 is hydrogen, substituted aliphatic residue having from 1 to 20 carbon atoms, an alkenyl or alkylnyl residue having from 2 to 20 carbon atoms, a cycloaliphatic residue having from 5 to 12 carbon atoms, an araliphatic residue having from 7 to 14 carbon atoms, or an heterocyclic residue, or R3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid or when n is 2, R3 is a divalent residue of heterocyclic diacyl residue or a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or a boric acid; or when n is 4, R3 is a tetraacyl residue derived from an aliphatic tetracarboxylic acid..].
.[.M. Compounds of the formula I wherein n is 1, 2 and 4 and when n is 1, R3 is an acyl group .]. ##STR47## .[.wherein R7 is hydrogen, a cycloaliphatic residue having from 5 to 12 carbon atoms or a heterocyclic residue or R3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid or when n is 2, R3 is a divalent residue of a heterocyclic diacyl or a sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or when n is 4, R3 is a tetraacyl residue derived from an aliphatic tetracarboxylic acid..].
.[.N..]. .Iadd.J. .Iaddend.Compounds of the formula I wherein when n is 1, R3 is an acyl group ##STR48## wherein R7 is an unsubstituted aliphatic residue having from 1 to 20 carbon atoms or an aromatic residue having from 6 to 20 carbon atoms and when n is 2, R3 is an divalent aliphatic or aromatic diacyl residue or the groups --CO-- or --COCO-- and when n is 3, R3 is a trivalent residue and is an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric, o-phosphorous or o-boric acid and when n is 4, R3 is a tetravalent residue of a tetraacyl residue derived from an aromatic tetracarboxylic acid or from o-silicic acid.
.[.O. Compounds of the formula I wherein when n is 1, R3 is an acyl group .]. ##STR49## .[.wherein R7 is an unsbustituted aliphatic residue having from 1 to 20 carbon atoms or an aromatic residue having from 6 to 12 carbon atoms and when n is 2, R3 is an divalent aliphatic or aromatic diacyl residue or the carbonyl group and when n is 3, R3 is a trivalent residue and is an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric o-phosphorous or o-boric acid and when n is 4, R3 is a tetravalent residue of a tetraacyl residue derived from an aromatic tetracarboxylic acid or from o-silicic acid..].
The following groups .[.P.]. .Iadd.K .Iaddend.and Q are sub-groups of the compounds of formula Ia.
.[.P..]. .Iadd.K. .Iaddend.Compounds of the formula Ia wherein n is 1 and R is hydrogen or a monovalent alicyclic residue having from 5 to 12 carbon atoms.
.[.Q..]. .Iadd.L. .Iaddend.Compounds of the formula Ia wherein when n is 1, R is a monovalent aliphatic residue having from 1 to 20 carbon atoms or a monovalent aromatic residue having from 6 to 20 carbon atoms and when n is 2, R is a divalent aliphatic residue having from 1 to 20 carbon atoms or a divalent aromatic residue having from 6 to 20 carbon atoms.
The following compounds of the formula I are also a group of compounds of the present invention. ##STR50## wherein n is 1, 2, 3 or 4; R1 is a monovalent residue and is an alkyl residue having from 1 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an alkenyl or alkynyl residue having from 3 to 20 carbon atoms, an aralkyl residue having from 7 to 9 carbon atoms, or a residue having the formula: ##STR51## wherein m is 1, 2 or 3, R4 is a hydrogen, methyl or phenyl residue, X2 is halogen, cyano, ##STR52## --COR5, --CO.OR5, --CO.SR5, --CONR5 R6 or CS.NR5 R6 and X1 is hydroxyl, halogen, cyano, ##STR53## --OR5, --O--CO.R5, OCSR5, --O.CO.NR5 R6, --CO.R5, --CO.OR5, --CO.SR5, --CO.NR5 R6, --CS.NR5 R6, or --SR5, wherein R5 is an alkylresidue having from 1 to 20 carbon atoms, an alkenyl residue having from 2 to 20 carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an aryl residue having from 6 to 11 carbon atoms, or when R5 is joined to a nitrogen atom, also hydrogen, and R6 is hydrogen or a nalkyl residue having from 1 to 4 carbon atoms, or R5 and R6 together with the nitrogen atom to which they are bound form a 5- or 6-membered ring which contains no other heteroatom or contains one or more other heteroatoms or R1 is an acyl group, an unsubstituted or N-substituted carbamoyl or thiocarbamoyl group; R.sub. 2 is an alkyl residue having from 1 to 4 carbon atoms, an alkenyl or alkynyl residue having 3 to 20, carbon atoms, a cycloalkyl residue having from 5 to 12 carbon atoms, an aryl residue having from 6 to 11 carbon atoms or an aralkyl residue having from 7 to 9 carbon atoms or also hydrogen; and when n is 1, R2 is a monovalent radical having the same significance as R1, with the proviso that only one of R1 and R3 can represent a unsaturated acyl group or R3 represents a monovalent group obtained by removing a hydroxyl group from a sulphinic acid, a sulphonic acid, a phosphorus containing acid or a boric acid, or R3 is an aryl residue or a residue having the formula: ##STR54## wherein R1 ' is hydrogen or R1 ' has the same significance as R1.
When n is 2, R3 is a divalent residue and is an alkylene residue having from 1 to 20 carbon atoms, an alkenylene residue having from 3 to 20 carbon atoms, an alkynylene residue having from 3 to 20 carbon atoms, an arylene residue having 6 to 14 carbon atoms, an aralkylene residue having from 8 to 14 carbon atoms or an aliphatic, aromatic or heterocyclic diacyl residue, an aliphatic or aromatic dicarbamoyl or dithiocarbamoyl, a carbonyl, sulphinyl or sulphonyl residue or a divalent residue obtained by removing two hydroxyl groups from a disulphonic acid, a phosphorus containing acid or a boric acid; when n is 3, R3 is a trivalent residue or an aliphatic or aromatic triacyl residue or a triacyl residue derived from o-phosphoric, o-phosphorous or o-boric acid or an alkanetriyl, an arenetriyl, or arenetriyltrialkylene group; and when n is 4, R3 is a tetravalent residue and is a tetravalent aliphatic residue or tetraacyl residue derived from an aliphatic or aromatic tetracarboxylic acid or from o-silicic acid or an alkanetetrayl group; as well as patial ethers, esters and carbamoyloxy and thiocarbamoyloxy compounds related to the fully reacted compounds of formula I.
The following compounds of the formula II are also a group of compounds of the present invention.[...]..Iadd.: .Iaddend. ##STR55## and their salts, wherein R' and R" are the same or different and each is a straight or branched alkyl group, having from 1 to 4 carbon atoms, or R' and R" together with the carbon atom to which they are attached form a cycloalkyl residue having from 5 to 12 carbon atoms; Y is an alkyl group having from 1 to 20 carbon atoms, preferably 1 to 4, carbon atoms, alkenyl having from 2 to 20 carbon atoms or an aralkyl residue having from 7 to 9 carbon atoms and n1 is 1 or 2; when n is 1, R is hydrogen or a monovalent aliphatic residue having from 1 to 20, preferably 6 to 20 carbon atoms, a monovalent alicyclic residue having from 5 to 12 carbon atoms, or a monovalent aromatic residue having from 6 to 20 carbon atoms; and when n is 2, R is a divalent aliphatic residue having from 1 to 20, preferably .[.1.]. .Iadd.4 .Iaddend.to 20, carbon atoms, and is unsubstituted or substituted or interrupted by one or more, preferably one, sulphur atom, a divalent alicyclic residue having from 5 to 12 carbon atoms or a divalent aromatic residue having from 6 to 20 carbon atoms.
Subgroups of the compounds of formula II are
a. Compounds wherein Y is methyl or
b. Compounds wherein n is 1 and R is a monvalent aliphatic, alicyclic or aromatic residue having from 6 to 20 carbon atoms and this group has the formula: ##STR56## wherein R10 and R11 are the same or different and each is an alkyl group having from 1 to 6 carbon atoms, A is ##STR57## or --CH2 CH2 -- and p is 0 1, or
c. Compounds wherein R10 and R11 are methyl, isopropyl or t-butyl groups or
d. Compounds wherein n is 2 and R is a methylene, 1,2-ethylene, 1,4-butylene, 1,8-n-octylene, 2,2,4-trimethyl-1, 4-butylene, 1,10-n-decylene, 1,2-eicosylene, vinylene, propenylene, 1,2-, 1,3- or 1,4-cyclohexylene, cyclohexyl-3-ene, 1,2-, 1,3- or 1,4-phenylene, p-xylylene, 1,4- or 1,5-naphthylene, diphenylene or diphenylmethylene residue or the group --CH2 CH2 S CH2 CH2 -- or R is absent.
e. Compounds in the form of its salt of an inorganic or organic acid.
f. Compounds wherein the salt is a phosphate, carbonate, sulphate, chloride, acetate, stearate, maleate, nitrate, tartrate, oxalate, benzoate or substituted carbamate.
G. Compounds wherein R' and R" are methyl.
The following compounds of the formula IV are also compounds of the present invention: ##STR58## and its salts wherein RIII and RIV are the same or different and each is a straight- or branched alkyl residue having from 1 to 12 carbon atoms or RIII and RIV together with the carbon atom to which they are each attached form a cycloalkyl group having from 5 to 12 carbon atoms, Y is a straight- or branched alkyl residue having from 1 to 12 carbon atoms, an alkenyl residue having from 3 to 12 carbon atoms or an aralkyl residue having from 7 to 12 carbon atoms and R12 is hydrogen or a saturated or unsaturated hydrocarbyl residue containing up to 20 carbon atoms optionally substituted, .[.Y.]. .Iadd.by .Iaddend.halogen or alkoxy having from 1 to 4 carbon atoms and q is 1 or 2. Sub-groups of the compounds of formula IV are:
a. Compounds wherein q is 1 and R12 is an aliphatic residue having from 1 to 20 carbon atoms, an alicyclic residue having from 5 to 12 carbon atoms or an aromatic residue having from 6 to 12 carbon atoms.
b. Compounds wherein R12 is a methyl, ethyl, propyl, isopropyl, n-butyl, 2-ethylhexyl, dodecyl, octadecyl, allyl, oleyl cyclohexyl, benzyl, phenyl o-, m- or p-tolyl, 2,4- or 2,6-xylyl or a naphthyl residue.
c. Compounds wherein q is 2 and R12 is an aliphatic residue having from 1 to 20 carbon atoms, an alicyclic residue having from 5 to 15 carbon atoms or an aromatic residue having from 6 to 15 carbon atoms.
d. Compounds wherein R12 is a 1,2-ethylene, 1,6-hexylene, 2,4,4-trimethyl-1,6-hexylene, 1,3- or 1,4-phenylene, 2,4-tolylene, 1,5-naphthylene or 4,4'-diphenylmethylene residue.
e. Compounds wherein Y1 is methyl.
f. Compounds in the form of its salt of an inorganic or organic acid.
g. Compounds wherein the salt is a phosphate, carbonate, sulphate, chloride, acetate, carbonate, sulphate, chloride, acetate, stearate, maleate, citrate, tertrate, oxalate, benzoate or substituted carbamate.
h. Compounds wherein RIII and RIV are methyl.
According to the present invention, there is also provided a first process in which a compound of formula I is produced, comprising reacting, in the presence of an acidbinding agent, a piperidinol having the formula: ##STR59## wherein R1 and R2 have their previous significance, with an acid halide having the formula:
.[.R.sub.3 --(CO hal).sub.n .]. .Iadd.R.sub.3 (hal).sub.n .Iaddend.VI
wherein R3 and n have their previous significance and hal represents a halogen atom, preferably a chlorine atom.
Suitable acid binding agents are organic bases such as triethylamine; alternatively, an excess amount of the amine V can serve as the acid binding agent.
The reaction is conveniently carried out by heating the reactants together in a solvent such as cyclohexane, benzene or toluene which is inert under the reaction conditions. When the reaction is complete, the desired product is then separated by conventional techniques.
The present invention also provides a second process in which a compound of formula I is produced, comprising reacting, in the presence of a transesterification catalyst, a piperidinol compound of formula V, as hereinbefore defined, with an ester having the formula:
.[.R.sub.3 --(CO.sub.2 R.sub.13).sub.N .]. .Iadd.R.sub.3 (OR.sub.13).sub.n .Iaddend.                                                 VII
wherein R3 and n have their previous significance and R13 is an alkyl residue having from 1 to 4 carbon atoms, preferably 1 or 2 carbon atoms.
Examples of suitable transesterification catalysts are alkali metal amides such as lithium amide.
A third process according to this invention in which a compound of formula I is produced comprises reacting, in the presence of an esterification catalyst, a pieridinol compound of formula V, as hereinbefore defined, with an acid having the formula:
.[.R.sub.3 (CO.sub.2 H).sub.n .]. .Iadd.R.sub.3 (OH).sub.n .Iaddend.VIII
wherein R3 and n have their previous significance.
Suitable examples of esterification catalysts are neutral catalysts such as tetraalkyl titanates such as tetrabutyl titanate.
The second and third processes of the invention are conveniently effected by mixing the reactants together in the presence or absence of an inert solvent (for instance, benzene, toluene, xylene etc.) and agitating the reaction mixture until reaction is complete, as determined, for instance, by collecting the alcohol or water produced in the reaction, and stopping the reaction when the theoretical amount of alcohol or water, respectively, has been removed.
A fourth process in which a compound of formula I is produced comprises reacting a compound having the formula: ##STR60## wherein R2, R3 and n have their previous significance, with a compound X capable of reaction with the compound IX and of introducing into it the group R1 as hereinbefore defined.
For instance, compound X may be an alkylating, alkenylating or aralkylating agent such as the halides of these groups. Compound X may also be the aldehyde or ketone corresponding to the substituent R1, so that, when reacted with a compound of formula IX under Leuckart, Wallach or Eschweilar-Charles reaction conditions, compounds of formula I in which R1 is methyl may be produced by reacting a compound of formula IX with formic acid and formaldehyde.
The starting-materials of formulae V, VI, VII, VIII, IX and X used in the process of this invention can all be produced by methods well-known per se. The compounds of formula V are described in our copending British Patent Application No. (Case 32/72) and those of formula IX are described generally in German Patent Specification No. 1,929,928.
Compounds of the general formula I in which .[.b.]..Iadd.n.Iaddend.=2, 3 or 4 and R3 represents a di-, tri- or tetra-valent radical derived from an alkyl, alkenyl, aryl or aralkyl radical may be prepared by reacting a compound of the formula: ##STR61## R1 and R2 has its previous significance, with a compound of the formula R3 (X4)n wherein X4 is a halogen atom and n is 2, 3 or 4. This reaction is preferably carried out by making the sodium salt of the piperidine compound and reacting this with the compound R3 (X4)n.
The substituents R1 may be introduced before or after R3 or in the case where R1 and R3 are identical may be introduced together by reacting a compound of the formula: ##STR62## with an alkylating, alkenylating, alkynylating, aralkylating, acylating agent or carbamoyloxyating agent, with an alkylating alkenylating, alkynylating, aralkylating or acylating agent.
Compounds of formula I in which R1 represents a residue of the formula: ##STR63## in which R4 is as defined above, m is 1 and X1 represents --CN, --OR5, ##STR64## R5 and R6 being as defined above, may be produced by reacting a compound of the formula: ##STR65## wherein R3 and R2 are as defined above, with a compound having the formula ##STR66##
Compounds of formula I wherein m is 1 and X1 is --OH may be prepared by reacting a compound of formula XII with ethylene oxide, propylene oxide or styrene oxide.
Compounds of formula I wherein R1 is ##STR67## wherein X1 is --OR5, ##STR68## or halogen may be prepared from the corresponding compounds wherein X1 is --OH by standard methods,
such as alkylation, esterification, carbamoyloxylation or halogenation.
Compounds of formula I in which R1 represents a residue of formula: ##STR69## wherein m, R4 and X1 are as hereinbefore defined may be prepared by reacting a compound of formula XII with the appropriate halogen compound having the formula: ##STR70## wherein X3 is a halogen atom.
Compounds of formula I in wich R1 is the group of formula: ##STR71## wherein X2 and R4 are as defined above may be prepared by reacting a compound of the formula XII wherein R2 is as defined above with a compound of the formula ##STR72## wherein X4 is a halogen atom.
Compounds of the general formula I in which R1 represents an acyl group may be prepared by reacting a compound of the formula: ##STR73## wherein R2 and R3 are as defined above with an acyl halide of the formula ##STR74## wherein X5 is a halogen, and R14 is the remainder of the acyl group.
Compounds of the general formula I in which R1 represents a carbamoyl or thiocarbamoyl group may be prepared by reacting a compound of the formula: ##STR75## R2 and R3 being as defined above with an isocyanate or thioisocyanate of the formula R15 NCX1 in which X1 is <O or <S, and R15 is the remainder of the isocyanate or thioisocyanate group.
Where R2 in the general formula I is other than hydrogen it is preferred to introduce the appropriate group before or after the group R1 is introduced, but before R3 is introduced. The group R2 may be introduced by reacting a ketone of the formula ##STR76## wherein R1 1 is hydrogen R1, with a Grignard reagent R2 MgX followed by hydrolysis to produce a compound of the formula: ##STR77##
All the reactions described above which result in the elimination of hydrogen halide between two reactants may be carried out in the presence of an acid acceptor.
Compounds of formula II as defined hereinbefore are produced by reacting, in the presence of an acid-binding agent, a piperidinol compound having the formula: ##STR78## wherein Y, R' and R" are as defined hereinbefore with an acid halide having the formula:
R--CO hal.).sub.n
whrein R and n are as defined hereinbefore and hal. represents a halogen atom. The acid binding agent can be an organic .Iadd.base .Iaddend.of an excess amount of the amine reactant XIV and the reactants are for example heated together in a solvent inert under the reaction conditions.
The process can be performed in the presence of a transesterification catalyst, such as an alkali metal, a piperidinol compound having the formula XIV, with an ester having the formula:
R--(CO.sub.2 R.sub.16).sub.n
wherein R and n are as defined above and R16 is an alkyl group having from 1 to 4 carbon atoms, or with an acid having the formula:
R--(CO.sub.2 H).sub.n
wherein R and n are as defined above.
The catalyst of producing compounds of the formula II can be a neutral catalyst such as tetraalkyl titanate.
In the process for producing compounds of the formula II the reactants can also be fused, the mass is agitated until reaction is complete and the reaction is stopped when the reaction is complete. The completion of the reaction is determined for example by collecting, respectively, the alcohol or water produced in the reaction, and stopping the reaction when the theoretical amount of water or alcohol has been removed.
Compounds of formula II are also produced by reacting an ester having the formula: ##STR79## wherein R, R', R" and n are as defined above with a compound capable of reacting with the ester XV such as an alkylating or aralkylating agent or an aldehyde or ketone corresonding to the substituent Y and of introducing into it the group Y as defined above.
Compounds having the formula IV as defined hereinbefore are produced by reacting a compound having the formula: ##STR80## wherein Y, RIII and RIV are as defined hereinbefore with an isocyanate having the formula:
R.sub.12 (NCO).sub.q
wherein R12 and q are as defined hereinbefore. The reaction can be effected in a solvent inert under the reaction conditions and in the presence of a strong base.
The present invention still further provides a composition comprising an organic material and a stabilising amount of a compound having the formula I, II or IV as hereinbefore defined.
Compounds of formula I, II exceptionally IV, have been found to impart to polyolefines an exeptionally high degree of stability towards deterioration normally induced by the effects of ultra-violet radiation or exposure to heat. Moreover, this improved stability is achieved without affecting the colour properties of the treated polyolefine. The stabilisers of the invention provide effective light and/or heat stabilisation, especially for low- and high-density polyethylene and polypropylene and polystyrene as well as polymers of butene-1, pentene-1, 3-methyl-butene-1, hexane-1, 4-methylpentene-1, 4-methylhexene-1 and 4,4-dimethylpentene-1, and also co- and ter-polymers of olefines, particularly of ethylene or propylene.
Other organic materials susceptible to degradiation by the effects of light and the properties of which are improved by the incorporation therein of a compound of formula I, II or IV, include natural and synthetic polymeric materials, for instance natural and synthetic rubbers, the latter including, for example, homo-, co- and ter-polymers of acrylonitrile, butadiene and styrene.
Specific synthetic polymers include polyvinyl chloride, polyvinylidene chloride and vinyl chloride co-polymers polyvinyl acetate as well as condensation polymers derived from ether, ester (derived from carboxylic sulphonic or carbonic acids), amide or urethane groupings. These polymers can, for instance, form the basis of surface coating media such as paints and lacquers having an oil or resin, for instance an alkyd or polyamide resin base.
The amount of the compound of formula I, II or IV, which is incorporated into the organic material in order to achieve maximal protection against degradation by light varies according to the properties of the organic material treated and according to the severity of the light radiation and to the length of exposure. However, for most purposes it is sufficient to use an amount of the compound of formula I, II or IV, within the range of from 0.01% to 5% by weight, more preferably within the range of from 0.1% to 2% by weight based on the weight of untreated organic material.
The compounds may be incorporated into the polymeric material by any of the known techniques for compounding additives with a polymer. For example, the compound and the polymer may be compounded in an internal mixer. Alternatively, the compound may be added as a solution or slurry in a suitable solvent or dispersant, for instance an inert organic solvent such as methanol, ethanol or acetone to powdered polymer and the whole mixed intimately in a mixer, and the solvent subsequently removed. As a further alternative the compound may be added to the polymer during the preparation of the latter, for instance at the latex stage of polymer production, to provide pre-stabilised polymer material.
Optionally, the composition of the invention may contain one or more further additives, especially those used in polymer formulations, such as antioxidants of the phenol or amine type, U.V. absorbers and light protectants, phosphite stabilisers, peroxide decomposers, polyamide stabilisers, basic co-stabilisers, polyvinyl chloride stabilisers, nucleation agents, plasticizers, lubricants, emulsifiers, anti-static agents, flame-protectants, pigments, carbon black, asbestos, glass fibres, kaolin and talc.
The present invention therefore includes binary, tertiary and multi-component compositions containing the stabiliser of formula I, II or IV, together with one or more functional additives for polymers.
Examples of suitable antioxidants are those of the hindered phenol type such as those selected from the following groups:
1. Phenolic compounds having the general formula
Q--(CH.sub.2).sub.w --A.sub.1
wherein Q is ##STR81## A1 is --CR(COOR")2 ##STR82## R is hydrogen or lower alkyl, R' is lower alkyl,
R" is alkyl group having from 6-24 carbon atoms, w is an integer from 0 to 4.
Illustrative examples of the compounds shown above are:
di-n-octadecyl-α-(3,5-di-t-butyl-4-hydroxy-benzyl)malonate
di-n-octadecyl-α-(3-t-butyl-4-hydroxy-5-methylbenzyl)malonate which is disclosed in the Netherlands Pat. No. 6,711,199, Feb. 19, 1968
di-n-octadecyl-α,α'bis-(3-t-butyl-4-hydroxy-5-methylbenzyl)malonate which is disclosed in the Netherlands Pat. No. 6,803,498, Sept. 18, 1968.
2. Phenolic compounds having the general formula
Q--R"'
Illustrative examples of the compounds shown above are:
2,6-di-t-butyl-p-cresol
2-methyl-4,6-di-t-butylphenol and the like
2,6-di-Octadecyl-p-cresol
3. Phenolic compounds having the formula
Q--C.sub.x H.sub.2x --Q
Illustrative examples of the compounds shown are:
2,2'-methylene-bis(6-t-butyl-4-methylphenol)
2,2'-methylene-bis(6-t-butyl-4-ethylphenol)
4,4'-butylidene-bis(2,6-di-t-butylphenol)
4,4'-(2-butylidene)-bis(2-t-butyl-5-methylphenol)
2,2'-methylene-bis[6-(2-t-methylcyclohexyl)]-4-methylphenol
2,2'-methylene-bis(3-t-butyl-5-ethylphenol)
4,4'-methylene-bis(3,5-di-t-butylphenol)
4,4'-methylene-bis(3-t-butyl-5-methylphenol)
2,2'-methylene-bis(3-t-butyl-5-methylphenol) and the like.
4. Phenolic compounds having the formula:
R"'--O--Q
Illustrative examples of such compounds are:
2,5-di-t-butylhydroquinone
2,6-di-t-butylhydroquinone
2,5-di-t-butyl-4-hydroxyanisole
5. Phenolic compounds having the formula:
Q--S--Q.
Illustrative examples of such compounds are:
4,4'-thiobis-(2-t-butyl-5-methylphenol)
4,4'-thiobis-(2-t-butyl-6-methylphenol)
2,2'-thiobis-(6-t-butyl-4-methylphenol)
4,4'-thiobis-(2-methyl-5-t-butylphenol)
6. Phenolic compounds having the formula ##STR83##
Illustrative examples of such compounds are:
octadecyl-(3,5-dimethyl-4-hydroxybenzylthio)-acetate
dodecyl-(3,5-di-t-butyl-4-hydroxybenzylthio)-propionate
7. Phenolic compounds having the formula ##STR84## wherein T is hydrogen R or Q as defined above.
Illustrative examples of such compounds are:
1,1,3-tris(3,5-dimethyl-4-hydroxyphenyl)-propane
1,1,3-tris(5-t-butyl-4-hydroxy-2-methylphenyl)-butane
1,1,5,5-tetrakis-(3'-t-butyl-4'-hyroxy-6'-methylphenyl)-n-pentane
8. Phenolic compounds having the formula: ##STR85## wherein B1, B2 and B3 are hydrogen, methyl or Q, provided that when B1 and B3 are Q then B2 is hydrogen or methyl and when B2 is Q then B1 and B3 are hydrogen or methyl.
Illustrative examples of such compounds are:
1,4-di(3,5-di-t-butyl-4-hydroxybenzl)-2,3,5,6-tetramethylbenzene
1,3,5-tri(3,5-di-t-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene
.[.8..]. .Iadd.9. .Iaddend.Phenolic compounds having the formula ##STR86## wherein Z is NHQ, --S--D--or --O--Q D is alkyl group having from 6-12 carbon atoms or --(Cw H2-w)--S--R"
Illustrative examples of such compounds are:
2,4-bis-(o-octylthio)-6-(3,5-di-t-butyl-4-hydroxyaniline)-1,3,5-triazine
6-(4-hydroxy-3-methyl-5-t-butylanilino)-2,4-bis-(n-octylthio)-1,3,5-triazine
6-(4-hydroxy-3,5-dimethylanilino)-2,4-bis-(n-octylthio)-1,3,5-triazine
6-(4-hydroxy-3,5-di-t-butylanilino)-2,4-bis-(n-octylthio)-1,3,5-triazine
6-(4-hydroxy-3,5-di-t-butylanilino)-4-(4-hydroxy-3,5-di-t-butylphenoxy)-2-(n-octylthio)1,3,5-triazine
2,4-bis(4-hydroxy-3,5-di-t-butylanilino)-6-(n-octylthio)-1,3,5-triazine
The above phenolic triazine stabilizers are more fully described in U.S. Pat. No. 3,255,191. 10. Phenolic compounds having the formula: ##STR87## wherein Z' is --O--Q, --S--D or --S--(C.sub.ω H2ω)--SD.
Illustrative examples of such compounds are:
2,3-bis-(3,5-di-t-butyl-4-hydroxyphenoxy)-6-(n-octylthio)-1,3,5-triazine
2,4,6-tris-(4-hydroxy-3,5-di-t-butylphenoxy)-1,3,5-triazine
6-(4-hydroxy-3,5-di-t-butylphenoxy)-2,4-bis-(n-octylthioethylthio)-1,3,5-triazine
6-(4-hydroxy-3-methylphenoxy)-2,4-bis-(n-octylthio)-1,3,5-triazine
6-(4-hydroxy-3-t-butylphenoxy)-2,4-bis-(n-octylthioethylthio)-1,3,5-triazine
6-(4-hydroxy-3-methyl-5-t-butylphenoxy)-2,4-bis-(n-octylthio)-1,3,5-triazine
2,4-bis-(4-hydroxy-3-methyl-5-t-butylphenoxy)-6-(n-octylthio)-1,3,5-triazine
2,4,6-tris(4-hydroxy-3-methyl-5-t-butylphenoxy)-1,3,5-triazine
6-(4-hydroxy-3,5-di-t-butylphenoxy)-2,4-bis-(n-octylthiopropylthio)-1,3,5-triazine
6-(4-hydroxy-3,5-di-t-butylphenoxy)-2,4-bis-(n-dodecylthioethylthio)-1,3,5-triazine
2,4-bis-(4-hydroxy-3,5-di-t-butylphenoxy)-6-butylthio-1,3,5-triazine
2,4-bis-(4-hydroxy-3,5-di-t-butylphenoxy)-6-(n-octadecylthio)-1,3,5-triazine
2,4-bis-(4-hydroxy-3,5-di-t-butylphenoxy)-6(n-dodecylthio)-1,3,5-triazine
2,4-bis-(4-hydroxy-3,5-di-t-butylphenoxy)-6-(n-octylthiopropylthio)-1,3,5-triazine
2,4-bis-(4-hydroxy-3,5-di-t-butylphenoxy)-6-(n-octylthioethylthio)-1,3,5-triazine
2,4-bis-(4-hydroxy-3,5-di-t-butylphenoxy)-6-(n-dodecylthioethylthio)-1,3,5-triazine.
The above phenolic triazine stabilizers are more fully described in U.S. Pat. No. 3,255,191.
11. Phenolic compounds having the formula
[Q--C.sub.z H.sub.2x --COO--C.sub.z H.sub.2x ].sub.p --R"'--(R).sub.4-p
wherein p is an integer from 2 to 4 and R"' is a tetravalent radical selected from aliphatic hydrocarbons having from 1 to 30 carbon atoms, aliphatic mono- and di-thioethers having from 1 to 30 carbon atoms, aliphatic mono- and diethers having from 1 to 30 carbon atoms and z is an integer from 0 to 6.
Illustrative examples of such compounds are
Sub-class I
.[.n-Octadecyl-.]. .Iadd.n-octadecyl-.Iaddend.3,-(3,5-di-t-butyl-4-hyroxyphenyl)-propionate
.[.n-Octadecyl-.]. .Iadd.n-octadecyl-.Iaddend.2-(3,5-di-t-butyl-4-hydroxyphenyl)-acetate
.[.n-Octadecyl-.]. .Iadd.n-octadecyl-.Iaddend.3,5-di-t-butyl-4-hydroxybenzoate
.[.n-Hexyl-.]. .Iadd.n-hexyl-.Iaddend.3,5-di-t-butyl-4-hydroxyphenylbenzoate
.[.n-Dodecyl-.]. .Iadd.n-dodecyl-.Iaddend.3,5-di-t-butyl-4-hydroxyphenylbenzoate
.[.Neo-dodecyl-.]. .Iadd.neo-dodecyl-.Iaddend.3-(3,5-di-t-butyl-4-hydroxphenyl)-propionate
.[.Dodecyl-.]. .Iadd.dodecyl-.Iaddend.β-(3,5-di-t-butyl-4-hydroxyphenyl)-propionate
.[.Ethyl.]. .Iadd.ethyl.Iaddend.-α-(4-hydroxy-3,5-di-t-butylphenyl)-isobutyrate
.[.Octadecyl.]. .Iadd.octadecyl.Iaddend.-α-(4-hydroxy-3,5-di-t-butylphenyl)-isobutylrate
.[.Octadecyl.]. .Iadd.octadecyl.Iaddend.-α-(4-hydroxy-3,5-di-t-butylphenyl)-propionate
Sub-Class II
2-(n-octylthio)ethyl 3,5-di-t-butyl-4-hydroxybenzoate
2-(n-octylthio)ethyl 3,5-di-t-butyl-4-hydroxyphenylacetate
2-(n-octadecylthio)ethyl 3,5-di-t-butyl-4-hydroxyphenylacetate
2-(n-octadecylthio)ethyl 3,5-di-t-butyl-4-hydroxybenzoate
2-(2-hydroxyethylthio)ethyl 3,5- di-t-butyl-4-hydroxybenzoate
2,2'-.[.Thiodiethanol.]. .Iadd.thiodiethanol .Iaddend.bis(3,5-di-t-butyl-4-hydroxyphenyl)acetate
.[.Diethyl.]. .Iadd.diethyl .Iaddend.glycol bis-[3,5-di-t-butyl-4-hydroxyphenyl)propionate]
2-(n-octadecylthio)ethyl 3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate
2,2'-.[.Thiodiethanol.]. .Iadd.thiodiethanol .Iaddend.-bis-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate
.[.Stearamido.]. .Iadd.stearamido .Iaddend.N,N-bis-[ethylene 3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]
.[.n-Butylimino.]. .Iadd.n-butylimino .Iaddend.N,N-bis-[ethylene 3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]
2-(2-stearoyloxyethylthio)ethyl 3,5-di-t-butyl-4-hydroxybenzoate
2-(2-hydroxyethylthio)ethyl 7-(3-methyl-5-t-butyl-4-hydroxyphenyl)heptanoate
2-(2-stearoyloxyethylthio)ethyl 7-(3-methyl-5-t-butyl-4-hydroxyphenyl)heptanoate
Sub-class III
1,2-propylene glycol bis-[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]
.[.Ethylene.]. .Iadd.ethylene .Iaddend.glycol bis-[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]
.[.Neopentylglycol.]. .Iadd.neopentylglycol .Iaddend.bis-[3-(3,5-di-t-butyl-4hydroxyphenyl)propionate]
.[.Ethylene.]. .Iadd.ethylene .Iaddend.glycol bis-(3,5-di-t-butyl-4-hydroxyphenylacetate)
.[.Glycerine.]. .Iadd.glycerine.Iaddend.-1-n-octadecanoate-2,3-bis-(3,5-di-t-butyl-4-hydroxyphenylacetate
.[.Pentaethylthritol.]. .Iadd.pentaethylthritol.Iaddend.-tetrakis-[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate
1,1,1-trimethylol ethane-tris-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate
.[.Sorbitol.]. .Iadd.sorbitol .Iaddend.hexa-[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate
1,2,3-butanetriol tris-[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]
2-hydroxyethyl 7-(3-methyl-5-t-butyl-4-hydroxyphenyl)heptanoate
2-stearoyloxyethyl 7-(3-methyl-5-t-butyl-4-hydroxyphenyl)heptanoate
1,6-n-hexanediol-bis](3',5'-di-t-butyl-4-hydroxyphenyl)propionate]
The above phenolic ester stabilizers of sub-classes I, II and III are more fully described in U.S. Pat. No. 3,330,859, Ser. No. 354,464, filed Mar. 24, 1964 and Ser. No. 359,460, filed Apr. 13, 1964, respectively.
12. Phenolic compounds having the formula ##STR88## where x is an integer of 1 or 2.
Illustrative examples of such compounds are
Di-n-octadecyl 3,5-di-t-butyl-4-hydroxybenzyl-phosphonate
Di-n-octadecyl 3-t-butyl-4-hydroxy-5-methylbenzylphosphonate
Di-n-octadecyl 1-(3,5-di-t-butyl-4-hydroxyphenyl)ethanephosphonate
Di-n-tetradecyl 3,5-di-t-butyl-4-hydroxybenzylphosphonate
Di-n-hexydecyl 3,5-di-t-butyl-4-hydroxybenzylphosphonate
Di-n-docosyl-3,5-di-t-butyl-4-hydroxybenzylphosphonate
Di-n-octadecyl 3,5-di-t-butyl-4-hydroxybenzylphosphonate.
The above di-(higher)alkyl phenolic phosphonates are more fully described in U.S. Pat. No. 3,281,505.
13. Phenolic compounds having the formula ##STR89## wherein W and Q are defined above.
Illustrative examples of such compounds are:
tris-(3,5-di-t-butyl-4-hydroxybenzyl)isocyanurate
tris-(3-t-butyl-4-hydroxy-5-methylbenzyl)isocyanurate.
The above hydroxyphenylalkenyl isocyanurates are more fully described in U.S. Pat. No. 3,531,483.
The above phenolic hydrogen stabilizers are known and many are commercially available.
While any of the above mentioned antioxidants can be useful in combination with the ultraviolet light stabilizers of this invention, the preferred antioxidants consist of the hindered phenols in groups 1, 8, 9, 10, 11, 12 and 13 as mentioned above. The most preferred hindered phenols are those of groups 1, 9, 11, 12 and 13.
Further examples of antioxidants are those of the aminoaryl series for instance aniline and naphthylamine derivatives as well as their heterocyclic derivatives such as:
phenyl-1-naphthylamine
phenyl-2-naphthylamine
N,N'-diphenyl-p-phenyldiamine
N,N'-di-sec.butyl-p-phenylenediamine
6-Ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline
6-Dodecyl-2,2,4-trimethyl-1,2-dihydroquinoline
mono- and di-octyliminodibenzyl and polymerised 2,2,4-trimethyl-1,2-dihydroquinoline. Ultraviolet absorbers and light protectants include
a. 2-(2'-hydroxyphenyl)benzotriazoles, for instance 5'-methyl; 3',5'-di-t-butyl; 5'-t-butyl; 5-chloro-3', 5'-di-t-butyl; 5-chloro-3'-t-butyl-5'-methyl; 3'-sec. butyl-5'-tert.butyl; 3'-[α-methylbenzyl]-5'-methyl-; 3'-[α-methylbenzyl)-5'-methyl-5-chloro-; 4'-octoxy-:; 3',5'-di-t-amyl; 3'-methyl-5'-carbamethoxyethyl; 5-chloro-3',5'-di-t-amyl derivatives.
b. 2,4-bis-(2'-hydroxyphenyl)-6-alkyl-S-triazines, for instance the 6-ethyl or 6-undecyl derivatives.
c. 2-hydroxybenzophenones, for instance the 4-hydroxy, 4-methoxy, 4-octoxy-, 4-decyloxy-, 4-dodecyloxy-, 4,2', 4'-trihydroxy or 2'-hydroxy-4,4'-dimethoxy derivatives.
d. 1,3-bis(2'-hydroxybenzoyl)-benzenes for instance, 1,3-bis-(2'-hydroxy-4'-hexyloxybenzoyl)benzene 1,3-bis-(2'-hydroxy-4'-octoxybenzoyl)benzene 1,3-bis-(2'-hydroxy-4'-dodecyloxybenzoyl)benzene
e. Aryl esters from optionally substituted benzoic acids such s phenylsalicylate, octylphenylsalicylate, dibenzoyl resorcino, bis-(4-tert.butylbenzoyl) resorcinol, benzoylresorcinol and 3,5-di-tert.butyl-4-hydroxybenzoic acid-2,4-di-tert.butyl phenyl ester and -octadecyl ester and -2-methyl-4,6-di-tert.butyl phenyl ester.
f. Acrylates, for instance
α-Cyano-β,β-diphenylacrylic acid ethyl- or iso-octyl ester, α-carbomethoxy-cinnamic acid, methyl- or butyl ester and N-(β-carbomethoxyvinyl)-2-methyl indoline.
g. Nickel compounds such as nickel complexes of 2,2'-thio-bis-(4-tert.octylphenol), for instance the 1:1 and 1:2 complexes, optionally having other ligands such as n-butylamine, triethanolamine or N-cyclohexyl-diethanolamine; nickel complexes of bis-(4-tert.octylphenyl) sulphone such as the 2:1 complex, optionally having other ligands such as 2-ethylcaproic acid; nickel dibutyl di-thiocarbamates; nickel salts of 4-hydroxy-3,5-di-tert. butylbenzyl-phosphonic acid mono-alkyl esters such as the methyl-, ethyl- or butyl esters; the nickel complex of 2-hydroxy-4-methyl-phenyl-undecylketonoxime; and nickel-3,5-di-tert.butyl-4-hydroxy benzoate, and
h. Oxalic acid diamides, for instance
4,4'-dioctyloxyoxanilide
2,2'-dioctyloxy-5,5'-di-tert.butyl-oxenilide
2,2'-di-dodecyloxy-5,5'-di-tert.butyl oxanilide
2-ethoxy-5-tertiarybutyl-2'-ethyl-oxanilide
2-ethoxy-2'-ethyl-oxanilide mixtures of o- and p-methoxy and ethoxy-di-substituted oxanilides and the compound of formula: ##STR90##
Phosphite stabilisers include triphenyl phosphite, diphenylalkyl phosphites, phenyl dialkyl phosphites, trinonylphenyl phosphite, trilauryl phosphite, trioctadecyl phosphite, 3,9-di-isodecyloxy-2,4,8,10-tetraoxa-3,9-diphosphaspiro-(5,5)-undecane and tri-(4-hydroxy-3,5-di-tert.butylphenyl)phosphite.
Peroxide-decomposing compounds for polyolefins include esters of β-thiodipropionic acids, for instance the lauryl-, stearyl-, myristyl- or tridecyl esters, salts of mercaptobenzimidazoles such as the zinc salt and diphenylthiourea.
Suitable polyamide stabilisers include copper salts in combination with iodides and/or further phosphorus compounds and salts of bivalent manganese.
Basic co-stabilisers are, for example, polyvinylpyrrolidone, melamine, benzoguanamine, triallyl cyanurate, dicyandiamide, urea derivatives, hydrazine derivatives, amines, polyamides, polyurethanes, alkali and alkaline earth salts of higher saturated or unsaturated fatty acids such as calcium stearate.
Polyvinyl chloride stabilisers include organotin compounds, organo lead compounds and Ba/Cd salts of fatty acids.
Examples of nucleation agents are 4-tert.butyl benzoic acid, adipic acid and diphenylacetic acid.
As with the compound of formula I, II or IV any further additive is advantageously employed in a proportion within the range of from 0.01% to 5% by weight, based on the weight of untreated polymeric material.
In binary combinations with one or more antioxidants listed above or in tertiary combinations with such antioxidants and U.V. absorbers listed above, the compounds of formula I, II or IV provide very effective stabiliser packages in polyolefine formulations.
Some Examples will now be given. Parts and percentages are by weight unless otherwise stated.
EXAMPLE 1
A mixture of 10.26 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol, 6.06 parts of sebacic acid and 1.0 parts of tetra-n-butyl titanate in 100 parts of xylene was heated under reflux conditions for 60 hours. Removal of the xylene by distillation under reduced pressure gave an oily solid which was heated under reflux conditions with 0.5 parts of sodium carbonate and 0.5 parts of carbon in 25 parts of water for 1 hour.
Removal of the water by distillation under reduced pressure gave a black residue which was repeatedly extracted with ether. The combined ether extracts were dried and the ether removed by distillation under reduced pressure to give a yellow oil which was distilled under reduced pressure to give 5.0 parts of bis(1,2,2,6,6-pentamethyl-4-piperidinyl) sebacate as a colourless oil having a boiling point of 220°-2° C. at 0.2 mm of Hg and the following elemental analysis by weight:
______________________________________                                    
         Found Required (for C.sub.30 H.sub.56 N.sub.2 O.sub.4)           
______________________________________                                    
Carbon     70.60%  70.82%                                                 
Hydrogen   11.00%  11.10%                                                 
Nitrogen    4.81%   5.51%                                                 
______________________________________
Table I gives a list of esters prepared using the procedure of Example 1.
TABLE I
  m.p. or ANALYSIS Example  b.p. Molecular REQUIRED (%) FOUND (%) No.
 R.sub.1 R.sub.2 R.sub.3 °C. at m.m. Formula C H N  C H N
                  2 CH.sub.3 H
  ##STR91##
  88° C. C.sub.21 H.sub.33 NO.sub.2 76.09 10.03 4.23  76.36 9.90
 3.99
  3 CH.sub.2CH.CH.sub.2 H
 ##STR92##
  130° C. at 0.05 m.m. Hg. C.sub.19 H.sub.23 NO.sub.2 74.22
 10.824.56  74.86 10.65 4.26
  4 CH.sub.3 H
 ##STR93##
  200° C. at0.1 m.m. Hg. C.sub.29 H.sub.23 NO.sub.2 77.18 12.26
 3.21  78.10 12.30 3.06
  5 CH.sub.3 H
 ##STR94##
  81-3° at0.05 m.m. Hg. C.sub.14 H.sub.27 NO.sub.2 69.67 11.27
 5.80  70.16 11.37 5.90
  6 CH.sub.3 H
 ##STR95##
  228-30° C. at0.1 m.m. Hg. C.sub.28 H.sub.30 N.sub.2 O.sub.2
 70.25 10.53 5.85  70.26 10.44 5.38
  7 CH.sub.3 H
 ##STR96##
  91-2° C. C.sub.34 H.sub.42 N.sub.2 O.sub.4 68.21 10.02 6.63
 68.05 9.97 6.47
  8 CH.sub.3 H
 ##STR97##
  210-20° C. at0.4 m.m. C.sub.26 H.sub.48 N.sub.2 O.sub.4 S 64.40
 9.98 5.78 S = 6.60 64.26 9.89 5.51 S = 6.59
  9 CH.sub.3 H
 ##STR98##
  61-5° C. C.sub.36 H.sub.46 N.sub.2 O.sub.2 S 68.99 10.69 6.19
 69.38 10.62 6.02
  10 CH.sub.3 H
 ##STR99##
  57° C. C.sub.19 H.sub.27 NO.sub.2 75.71 9.03 4.65  75.50 8.97
 4.71
  11 CH.sub.3 H
 ##STR100##
  120° C. at0.2 m.m. Hg. C.sub.18 H.sub.27 NO.sub.2 74.70 9.40
 4.84  74.99 9.70 4.85
  12 CH.sub.3 H
 ##STR101##
  148° C. at0.4 m.m. Hg. C.sub.19 H.sub.27 NO.sub.2 74.70 9.40
 4.84  74.98 9.42 4.70
  13 CH.sub.3 H
 ##STR102##
  51° C. C.sub.18 H.sub.27 NO.sub.3 70.79 8.91 4.59  70.49 8.71
 4.50
  14 CH.sub.3 H
 ##STR103##
  147° C. at0.1 m.m.Hg. C.sub.17 H.sub.24 NO.sub.2 Cl 66.00 7.81
 4.52 Cl = 11.44 65.98 7.65 4.53 Cl = 11.56
  15 CH.sub.3 H
 ##STR104##
  152-4° C. at0.2 m.m. Hg. C.sub.17 H.sub.24 NO.sub.2 Cl 66.00
 7.81 4.52 Cl = 11.44 65.89 7.65 4.53 Cl = 11.56
  16 CH.sub.3 H
 ##STR105##
  100° C. at0.2 m.m. Hg. C.sub.19 H.sub.26 NO.sub.2 72.68 11.68
 4.71  72.53 11.96 4.50
  17 CH.sub.3 H
 ##STR106##
  65° C. at0.4 m.m. Hg C.sub.13 H.sub.23 NO.sub.2 69.29 10.29 6.22
  69.64 10.30 6.15
  18 CH.sub.3 H
 ##STR107##
  196° C. at12 m.m. Hg C.sub.17 H.sub.25 NO.sub.3 74.14 9.15 5.09
 74.35 9.23 5.13
  19 CH.sub.3 H
 ##STR108##
  180° C. at0.5 m.m. Hg C.sub.17 H.sub.31 NO.sub.2 72.55 11.10
 4.98  72.84 11.04 4.77
  20 CH.sub.3 H
 ##STR109##
   44° C. C.sub.28 H.sub.35 NO.sub.2 76.83 12.66 3.20  76.71 12.35
 3.22
  21 CH.sub.3 H
 ##STR110##
  116-17° C. at0.2 m.m. Hg C.sub.18 H.sub.35 NO.sub.2 72.68
 11.864.71  72.56 11.50 4.99
  22 CH.sub.2CH.CH.sub.2 H
 ##STR111##
  129-30° C. at0.05 m.m. Hg C.sub.17 H.sub.25 NO.sub.3 70.07 8.65
 4.81  70.70 8.86 4.42
  23 CH.sub.3 H
 ##STR112##
  41-2° C. C.sub.30 H.sub.56 NO.sub.2 77.36 12.77   75.84 12.25
 24
  ##STR113##
  H
  ##STR114##
  183-5° C. at0.1 m.m. Hg C.sub.24 H.sub.30 NO.sub.2 77.16 10.52
 3.75  77.43 10.39 3.54
  25
 ##STR115##
  H
  ##STR116##
  55-6° C. C.sub.34 H.sub.56 NO.sub.2 79.47 11.57 2.73  79.32
 11.59 2.45
  26 CH.sub.3 H
 ##STR117##
  174-8° C. at0.1 m.m. Hg C.sub.22 H.sub.29 NO.sub.2 77.84 8.61
 4.13  78.35 8.63 4.12  27 CH.sub.3
  (CH.sub.2).sub.11 H
 ##STR118##
  190° C. at0.05 m.m. Hg C.sub.29 H.sub.57 NO.sub.2 77.10 12.72
 3.10  77.20 13.02 3.08
  28 CH.sub.3 H
 ##STR119##
  69-70° C. C.sub.24 H.sub.31 NO.sub.2 78.87 8.55 3.83  79.38 8.80
 3.69
  29 CH.sub.3 H
 ##STR120##
  90° C. at0.1 m.m. Hg C.sub.15 H.sub.29 NO.sub.2 70.54 11.45 5.48
  69.99 11.24 5.25  30 CH.sub.3
  (CH.sub.2).sub.11 H
 ##STR121##
  56° C. C.sub.28 H.sub.46 NO.sub.2 Cl 72.60 9.90 3.02 Cl = 7.66
 71.98 10.19 3.01Cl = 7.35
  31 CH.sub.3 H
 ##STR122##
  200° C. at0.2 m.m. Hg C.sub.34 H.sub.47 NO.sub.2 S 69.70 11.45
 3.39  69.69 11.48 3.31
  32 CH.sub.3 H
 ##STR123##
  119° C. C.sub.21 H.sub.36 NO.sub.2 75.63 10.58 4.20  75.94 10.30
 3.93         33 CH.sub.3
  (CH.sub.2).sub.17 H
 ##STR124##
  Purified bychroma-tography C.sub.34 H.sub.58 NO.sub.2 MOLECULAR WEIGHT
 = 513FOUND (FROM MASS SPECTROMETRY =
  513)
EXAMPLE 34
A solution of 17.10 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol in 50 parts of dry benzene was stirred at 15°-20° C. whilst adding 6.0 parts of sebacoyl chloride dropwise over 15 minutes. The mixture was stirred for a further 12 hours at room temperature after which the 1,2,2,6,6-pentamethylpiperidin-4-ol hydrochloride formed during the reaction was filtered off. The benzene was removed by distillation under reduced pressure to give a yellow oil, which was distilled under reduced pressure to give bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)sebacate as a colourless oil having a boiling point of 218°-20° C. at 0.4 mm of Hg and the following elemental analysis by weight:
______________________________________                                    
         Found  Required (for C.sub.30 H.sub.56 N.sub.2 O.sub.4)          
______________________________________                                    
Carbon     70.99%   70.82%                                                
Hydrogen   10.97%   11.10%                                                
Nitrogen   5.26%    5.51%                                                 
______________________________________
Table 2 gives a list of esters prepared using the procedure of Example 34.
                                  TABLE 2                                 
__________________________________________________________________________
                       m.p. or       ANALYSIS                             
                       b.p.   Molecular                                   
                                     Required (%)                         
                                              Found (%)                   
Example                                                                   
     R.sub.1                                                              
        R.sub.2                                                           
          R.sub.3      °C. at m.m.                                 
                              Formula                                     
                                     C  H  N  C  H  N                     
__________________________________________________________________________
35   CH.sub.3                                                             
        H                                                                 
           ##STR125##  Purified by chroma- tography                       
                              C.sub.26 H.sub.42 N.sub.2 O.sub.4 S         
                                           5.86     5.64                  
  36 CH.sub.3                                                             
        H                                                                 
           ##STR126##  118° C.                                     
                              C.sub.22 H.sub.40 N.sub.2 O.sub.4           
                                     66.63                                
                                        10.17                             
                                           7.06                           
                                              66.94                       
                                                 10.22                    
                                                    6.95                  
  37 CH.sub.3                                                             
        H                                                                 
           ##STR127##  123° C.                                     
                              C.sub.28 H.sub.44 N.sub.2 O.sub.4           
                                     70.15                                
                                        9.38                              
                                           5.93                           
                                              70.75                       
                                                 9.68                     
                                                    5.69                  
  38 CH.sub.3                                                             
        H                                                                 
           ##STR128##  75-6° C.                                    
                              C.sub.21 H.sub.27 NO.sub.2                  
                                     77.50                                
                                        8.36                              
                                           4.30                           
                                              77.78                       
                                                 8.45                     
                                                    4.06                  
  39 CH.sub.3                                                             
        H                                                                 
           ##STR129##  138° C. at 12 m.m. Hg.                      
                              C.sub.12 H.sub.23 NO.sub.2                  
                                     67.57                                
                                        10.87                             
                                           6.57                           
                                              67.90                       
                                                 10.72                    
                                                    6.53                  
  40 CH.sub.3                                                             
        H                                                                 
           ##STR130##  142° C.                                     
                              C.sub.25 H.sub.41 NO.sub.3                  
                                     74.40                                
                                        10.24                             
                                           3.47                           
                                              74.80                       
                                                 9.99                     
                                                    3.43                  
__________________________________________________________________________
EXAMPLE 41
A mixture of 17.10 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol, 13.60 parts of methyl benzoate and 2.0 parts of lithium amide was heated at 160° C. for six hours with removal of the methyl alcohol formed by distillation. Water pump vacuum was applied and heating continued for a further two hours; on cooling the residue was dissolved in chloroform and filtered to remove the lithium amide. The chloroform was removed by distillation under reduced pressure to give a yellow oil which was fractionally distilled under reduced pressure to yield 6.40 parts of 1,2,2,6,6-pentamethylpiperidinyl-4-benzoate having a boiling point of 126° C. at 0.1 mm of Hg. and the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.17 H.sub.25 NO.sub.2)                       
______________________________________                                    
Carbon        74.35%   74.14%                                             
Hydrogen      9.23%    9.15%                                              
Nitrogen      5.13%    5.09%                                              
______________________________________
EXAMPLE 42
A mixture of 17.10 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol, 14.60 parts of methyl-β-(3,5-di-t-butyl-4-hydroxyphenyl) propionate and 1.0 part of lithium amide was heated together to 130° C. Water pump vacuum was then applied to the reaction mixture whilst maintaining the temperature at 125°-135° C. for 3 hours. The temperature of the reaction mixture was then raised to 160° C. and high vacuum (0.5-1 mm Hg) was applied for 1 hour. The reaction mixture was cooled, dissolved in chloroform and filtered. Removal of the chloroform by distillation under reduced pressure gave a brown oil which, when triturated with ether, gave a white solid which was collected by filtration, washed will with ether and dried to give 16.0 parts of 1,2,2,6,6-pentamethylpiperidinyl-4-β-(3',5'di-t-butyl-4'-hydroxyphenyl)propionate as its bicarbonate salt having a melting point of 210°-11° C., and the following elemental analysis by weight:
______________________________________                                    
          Found  Required (for C.sub.27 H.sub.47 NO.sub.3)                
______________________________________                                    
Carbon      68.90%   68.10%                                               
Hydrogen    9.56%    9.60%                                                
Nitrogen    2.91%    2.84%                                                
______________________________________
EXAMPLE 43
15.0 parts of the product from Example 2 were dissolved in water and neutralised with sodium hydroxide solution. The aqueous solution was extracted with ether, the combined ether extracts were dried over anhydrous magnesium sulphate. The ether was removed by distillation under reduced pressure to give a white solid which was recrystallised from ethanol to give 9.30 parts of 1,2,2,6,6-pentamethylpiperidinyl-4-β-(3',5'-di-t-butyl-4'-hydroxyphenyl) propionate having a melting point of 124°-5° C. and the following elemental analysis by weight:
______________________________________                                    
         Found   Calculated (for C.sub.27 H.sub.45 NO.sub.3)              
______________________________________                                    
Carbon     75.00     75.30                                                
Hydrogen   10.50     10.20                                                
Nitrogen    3.50      3.30                                                
______________________________________
EXAMPLE 44
A mixture of 10.26 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol, 5.04 parts of trimethyl, trimesate and 0.20 parts of lithium amide in 100 parts of xylene was heated at 137° C. for 7 hours. The methyl alcohol formed during the reaction being removed by distillation. The cooled reaction mixture was filtered to remove the lithium amide and the xylene solvent removed by distillation under reduced pressure. Purification of the residue by preparative thin layer chromatography yielded dimethyl(1,2,2,6,6-pentamethylpiperidinyl-4) trimesate having the following molecular weight:
______________________________________                                    
Found (from mass spectrometry)                                            
                      391                                                 
Required (for C.sub.21 H.sub.22 NO.sub.3)                                 
                      391                                                 
______________________________________
and methylbis(1,2,2,6,6-pentamethylpiperdinyl-4) trimesate having the following molecular weight:
______________________________________                                    
Found (from mass spectrometry)                                            
                      530                                                 
Required (for C.sub.30 H.sub.46 N.sub.2 O.sub.3                           
                      530                                                 
______________________________________
EXAMPLE 45
A mixture of 16.4 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol, 6.27 parts of methyl isocyanate and 0.5 parts of 1,4-diazabicyclo[2,2,2]octane was refluxed in 150 parts of dry benzene for 24 hours. Removal of the benzene solvent by distillation under reduced pressure yielded an oily solid which was poured on to 200 parts of water and allowed to stand for 24 hours. The solid formed was collected by filtration, dried and crystallised from n-hexane to give 14.2 parts of 4-methylcarbamoyloxy-1,2,2,6,6-pentamethylpiperidine having a melting point of 96°-7° C. and the following elemental analysis by weight:
Table 3 gives a list of carbamoyloxy esters prepared using the procedure of Example 45.
______________________________________                                    
         Found   Required (for C.sub.12 H.sub.24 N.sub.2 O.sub.2)         
______________________________________                                    
carbon     63.28%    63.12%                                               
hydrogen   10.70%    10.59%                                               
nitrogen   12.09%    12.27%                                               
______________________________________                                    

  m.p. or  ANALYSIS b.p. Molecular Required (%) Found (%) Example R.sub.1 R
 .sub.2 R.sub.3 °C. at m.m. Formula C H N C H N
              46 CH.sub.3 H
  ##STR131##
  63° C. C.sub.17 H.sub.34 N.sub.2 O.sub.2 68.41 11.48 9.39 68.17
 11.32 9.16
  47 CH.sub.3 H
 ##STR132##
  56-7° C. C.sub.29 H.sub.58 N.sub.2 O.sub.2 74.62 12.52 6.00
 74.58 12.34 5.96
  48 CH.sub.3 H
 ##STR133##
  62° C. C.sub.14 H.sub.26 N.sub.2 O.sub.2 66.11 10.30 11.01 66.40
 10.27 10.92
  49 CH.sub.3 H
 ##STR134##
  184-6° C. at2 m.m. Hg. C.sub.17 H.sub.32 N.sub.2 O.sub.2 68.88
 10.88 9.45 68.98 10.84 9.43
  50 CH.sub.3 H
 ##STR135##
  109-10° C. C.sub.17 H.sub.26 N.sub.2 O.sub.2 70.31 9.02 9.65
 70.61 8.80 9.53
  51 CH.sub.3 H
 ##STR136##
  106-7° C. C.sub.18 H.sub.28 N.sub.2 O.sub.2 71.02 9.27 9.20
 71.42 9.41 9.02
  52 CH.sub.3 H
 ##STR137##
  121° C. C.sub.17 H.sub.25 N.sub.2 O.sub.2 Cl 62.86 7.70 8.68
 62.92 7.75 8.87
  53 CH.sub.3 H
 ##STR138##
  129° C. C.sub.21 H.sub.28 N.sub.2 O.sub.2 74.08 8.29 8.23 74.37
 8.07 8.41
  54 CH.sub.3 H
 ##STR139##
  101-4° C. C.sub.28 H.sub.54 N.sub.4 O.sub.4 65.84 10.66 10.97
 65.86 10.40 10.64
  55 CH.sub.3 H
 ##STR140##
  163-5° C. C.sub.29 H.sub.48 N.sub.4 O.sub.4 67.41 9.36 10.84
 67.21 9.52 10.83
  56 CH.sub.3 H
 ##STR141##
  183° C. C.sub.35 H.sub.52 N.sub.4 O.sub.4 70.91 8.84 9.45 70.64
 8.79 9.24
  57 CH.sub.3 H
 ##STR142##
  178° C. C.sub.32 H.sub.48 N.sub.4 O.sub.4 69.53 8.75 10.14 70.39
 8.71 9.86
  58 CH.sub.2 CH.CH.sub.2 H
 ##STR143##
  165° C. at0.05 m.m. Hg C.sub.19 H.sub.34 N.sub.4 O.sub.4 70.76
 10.63 8.69 70.64 10.80 9.04
  59 CH.sub.2CH.CH.sub.2 H
 ##STR144##
   60 CH.sub.3 CH.sub.2
  CH.sub.2 H
 ##STR145##
     61
 ##STR146##
  ##STR147##
EXAMPLE 62
A mixture of 28.3 parts of 2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate and 8.55 parts of benzyl bromide was stirred and heated at 105° C. for 72 hours. Ether was added to the cooled reaction mixture and the 2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate hydrobromide formed during the reaction was filtered off. The ether solvent was removed by distillation under reduced pressure and the residue distilled under reduced pressure to give 16.40 parts of 1-benzyl-2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate having a boiling point of 180° C. at 0.1 mm of Hg and the following elemental analysis by weight:
______________________________________                                    
                  Required                                                
            Found (for C.sub.24 H.sub.30 NO.sub.2)                        
______________________________________                                    
Carbon        77.46%  77.16%                                              
Hydrogen      10.50%  10.52%                                              
Nitrogen       3.86%   3.75%                                              
______________________________________
Table 4 gives a list of esters prepared using the procedure of Example 62. l
TABLE 4
  m.p. or  ANALYSIS Example  b.p. Molecular REQUIRED (%) FOUND (%) No.
 R.sub.1 R.sub.2 R.sub.3 °C. at m.m. Formula C H N C H N
               63
  ##STR148##
  H
  ##STR149##
  98-9° C. C.sub.42 H.sub.64 N.sub.2 O.sub.4 76.32 9.76 4.24 76.04
 9.49 4.04
  64
 ##STR150##
  H
  ##STR151##
  191-2° C. at0.1 m.m. Hg C.sub.21 H.sub.31 NO.sub.3 66.82 8.28
 3.71 66.81 8.52 3.84
  65 CH.sub.2CHCH.sub.2 H
 ##STR152##
  142-4° C. at0.2 m.m. Hg C.sub.20 H.sub.37 NO.sub.2 74.25 11.53
 4.33 74.06 11.36 4.32
  66
 ##STR153##
  H
  ##STR154##
  68-9° C. C.sub.20 H.sub.27 NO.sub.3 72.92 8.26 4.25 72.82 8.28
 4.55
  67 CH.sub.2CHCH.sub.2 H
 ##STR155##
  150° C. at0.05 m.m. Hg C.sub.18 H.sub.27 NO.sub.3 75.71 9.03
 4.65 75.58 9.25 4.45
  68 CH.sub.2CHCH.sub.2 H
 ##STR156##
  250° C. at0.5 m.m. Hg C.sub.34 H.sub.60 N.sub.2 O.sub.4 72.81
 10.78 4.99 73.07 10.60 4.77
  69
 ##STR157##
  H
  ##STR158##
  139-42° C.at 0.2 m.m. Hg C.sub.19 H.sub.33 NO.sub.3 70.55 10.28
 4.33 70.37 10.38 4.39
EXAMPLE 70
A mixture of 17.10 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol and 3.50 parts of metallic sodium in 125 parts of toluene was heated under reflux conditions for 24 hours. The toluene solution was decanted off from the excess sodium and then refluxed for a further 24 hours with 36.60 parts of n-octadecyl bromide. The cooled solution was filtered to remove the sodium bromide which was formed during the reaction and the toluene solvent was removed by distillation under reduced pressure. Fractional distillation of the residue gave 4-octadecyloxy-1,2,2,6,6-pentamethylpiperidine having a boiling point of 184° C. at 0.25 m.m. of Hg. and the following elemental analysis by weight:
______________________________________                                    
2                  Required                                               
            Found  (for C.sub.28 H.sub.57 NO)                             
______________________________________                                    
Carbon        78.66%   79.36%                                             
Hydrogen      13.77%   13.56%                                             
Nitrogen      2.99%    3.31%                                              
______________________________________
Table 5 gives a list of ethers prepared using the procedure of Example 70.
                                  TABLE 5                                 
__________________________________________________________________________
                    m.p. or         ANALYSES                              
Example             b.p.    Molecular                                     
                                    REQUIRED (%)                          
                                             FOUND (%)                    
No.  R.sub.1                                                              
        R.sub.2                                                           
            R.sub.3 °C. at m.m. Hg                                 
                            Formula C  H  N  C  H  N                      
__________________________________________________________________________
71   CH.sub.3                                                             
        H CH.sub.2CH.CH.sub.2                                             
  72 CH.sub.3                                                             
        H                                                                 
           ##STR159##                                                     
  73 CH.sub.3                                                             
        H CH.sub.3 (CH.sub.2).sub.11                                      
74   CH.sub.3                                                             
        H (CH.sub.2).sub.1                                                
                    m.p.                                                  
                       62-63                                              
                             .[.C.sub.24 H.sub.48 N.sub.2 U.sub.2         
                                    72.74                                 
                                       12.09                              
                                          7.07                            
                                             73.00                        
                                                11.94                     
                                                   6.85                   
                            .Iadd.C.sub.24 H.sub.48 N.sub.2 O.sub.2.Iadden
                            d.                                            
75   CH.sub.3                                                             
        H .[.(HCCH.sub.2.]. CH.Iadd.CCH.sub.2                             
                    b.p.                                                  
                       0.3 mm                                             
                            C.sub.13 H.sub.23 NO                          
                                    74.59                                 
                                       11.07                              
                                          6.69                            
                                             74.48                        
                                                10.95                     
                                                   6.41                   
                       73-74                                              
76   CH.sub.3                                                             
        H CH.sub.2 (CH.sub.2).sub.3                                       
                    b.p.                                                  
                       19 mm                                              
                            C.sub.14 H.sub.29 NO                          
                                    73.95                                 
                                       12.85                              
                                          6.16                            
                                             74.05                        
                                                12.93                     
                                                   6.10                   
                       123-124                                            
__________________________________________________________________________
EXAMPLE 77
3.23 Parts of 1-allyl-2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate in 50 parts of ethyl alcohol was hydrogenated at room temperature and 1 atmosphere pressure using 0.1 parts of 5% palladium on charcoal at the catalyst. The reaction mixture was filtered to remove the catalyst and the ethyl alcohol removed by distillation under reduced pressure to give 2.90 parts of 1-n-propyl-2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate having a boiling point of 128° C. at 0.05 mm of Hg and the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.20 H.sub.36 NO.sub.2)                       
______________________________________                                    
Carbon        73.50%   73.79%                                             
Hydrogen      12.26%   12.08%                                             
Nitrogen      4.31%    4.30%                                              
______________________________________
Table 6 gives a list of compounds prepared using the procedure of Example 77.
                                  TABLE 6                                 
__________________________________________________________________________
                       m.p. or    ANALYSIS                                
Example                b.p. Molecular                                     
                                  REQUIRED (%)                            
                                            FOUND (%)                     
No.  R.sub.1 R.sub.2                                                      
               R.sub.3 °C. m.m.                                    
                            Formula                                       
                                  C  H   N  C H  N                        
__________________________________________________________________________
78   CH.sub.3 CH.sub.2 CH.sub.2 --                                        
             H CH.sub.3 CH.sub.2 CH.sub.2 --                              
79   CH.sub.3                                                             
             H CH.sub.3 CH.sub.2 CH.sub.2 --                              
__________________________________________________________________________
EXAMPLE 80
a. A mixture of 2.83 parts of 2,2,6,6-.[.pentamethyl.]. .Iadd.tetramethyl.Iaddend.-4-piperidinyl-n-octanoate and 1.50 parts by volume of liquid ethylene oxide was charged into a 50 ml autoclave previously cooled to -50° C. A pressure of 100 atmospheres of nitrogen was applied and the autoclave heated at 200° C., with stirring, for three hours. Fractional distillation of the cooled reaction mixture yielded 2.30 parts of 1-(2'-hydroxyethyl)-2,2,6,6-tetramethyl)-4-piperidinyl-n-octanoate having a boiling point of 186°-7° C. at 0.25 mm of Hg and the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.10 H.sub.37 NO.sub.3)                       
______________________________________                                    
Carbon        69.93%   69.68%                                             
Hydrogen      11.09%   11.39%                                             
Nitrogen      4.37%    4.28%                                              
______________________________________
b. A mixture of 11.32 parts of 2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate and 2.50 parts of 2-bromoethanol was stirred at 100° C. for 65 hours. Petroleum ether (bp 40°-60° C.) was added to the cooled reaction mixture of the 2,2,6,6-tetramethylpiperidinyl-4-n-octanoate hydrobromide formed during the reaction was filtered off. The petroleum ether solvent was removed by distillation under reduced pressure and the residue distilled to yield 1-(2'-hydroxyethyl)-2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate having a boiling point of 176° C. at 0.2 mm of Hg. This sample was identical to that prepared under Example 80a.
EXAMPLE 81
A mixture of 11.45 parts of 4-phenylcarbamoyloxy-2,2,6,6-tetramethylpiperidine and 60 parts of styrene .[.ocide.]. .Iadd.oxide .Iaddend.in 60 parts of n-hexanol was heated under reflux conditions for 18 hours. The n-hexanol solvent and unreacted styrene oxide were removed by distillation under reduced pressure to yield a pale yellow crystalline solid. Purification by trituration with hot petroleum ether (b.p. 60°-80° C.) yielded 4-phenylcarbamoyloxy-1-[2'-hydroxy-2-'phenylethyl]-2,2,6,6-tetramethylpiperidine having a melting point of 186°-7° C. with the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.24 H.sub.32 N.sub.2 O.sub.3)                
______________________________________                                    
Carbon        72.51%   72.70%                                             
Hydrogen      7.92%    8.13%                                              
Nitrogen      6.91%    7.06%                                              
______________________________________
EXAMPLE 82
A mixture of 5.61 parts of 2,2,6,6-tetramethyl-4-piperidin-n-octanoate and 5.0 parts of propylene oxide were charged to an autoclave. A pressure of 100 atmospheres nitrogen was applied. The mixture was heated at 200° C. for 3 hours. Fractionation under reduced pressure gave a main fraction b.p. 160°-183° C. at 0.1 mm. which after passing down an alumina type II column eluting with chloroform yielded a pale yellow semi-solid 1-(2'-hydroxypropyl)-2,2,6,6-tetramethyl-4-piperidin-n-octanoate having the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.20 H.sub.30 NO.sub.3)                       
______________________________________                                    
Carbon        70.20%   70.34%                                             
Hydrogen      11.45%   11.51%                                             
Nitrogen      3.89%    4.10%                                              
______________________________________
EXAMPLE 83
A mixture of 3.27 parts of the product from 80 a., 0.60 parts of acetic acid and 0.1 parts of tetra-n-butyl titanate in 40 parts of xylene was heated under reflux conditions for 24 hours. The xylene solvent was removed by distillation under reduced pressure and the residue fractionally distilled to give 1-(2'-acetoxyethyl)-2,2,6,6-tetamethyl-4-piperidinyl-n-octanoate having a boiling point of 190°-2° C. at 1 m.m. Hg and the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.21 H.sub.30 NO.sub.4)                       
______________________________________                                    
Carbon        68.17%   68.25%                                             
Hydrogen      10.65%   10.64%                                             
Nitrogen      3.36%    3.79%                                              
______________________________________
EXAMPLE 84
A mixture of 3.27 parts of the product from Example .[.78.]. .Iadd.80 .Iaddend.a., 0.63 parts of methyl isocyanate and 0.1 parts of 1,4-diazabicyclo[2,2,2] octane in 30 parts of dry benzene was heated under reflux conditions for 24 hours. The benzene solvent was removed by distillation under reduced pressure and the residue crystallised from aqueous ethyl alcohol to give 1-(2'-.[.methylcarbonoyloxyethyl.]. .Iadd.methylcarbanoyloxyethyl.Iaddend.)-2,2,6,6-tetramethyl-4-piperidinyl-n-octanoate having a melting point of 61°-3° C. and the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.21 H.sub.40 N.sub.2 O.sub.4)                
______________________________________                                    
Carbon        65.72%   65.59%                                             
Hydrogen      10.37%   10.48%                                             
Nitrogen      7.11%    7.28%                                              
______________________________________
EXAMPLE 85
A mixture of 3.0 parts of the products from Example 81, 0.90 parts of phenyl isocyanate and 0.1 parts of 1,4-diazabicyclo[2,2,2]octane in 25 parts of dry benzene was heated under reflux conditions for 24 hours. The benzene solvent was removed by distillation under reduced pressure and the residue crystallised from petroleum ether (b.p. 60°-80° C.) to give 4-phenylcarbamoyloxy-1-[2'-(phenylcarbamoyloxy)-2'-phenylethyl]-2,2,6,6-tetramethylpiperidine having a melting point of 173° C. and the following elemental analysis by weight
______________________________________                                    
                   Required                                               
            Found  (for C.sub.31 H.sub.37 N.sub.3 O.sub.4)                
______________________________________                                    
Carbon        72.75%   72.21%                                             
Hydrogen      7.22%    7.23%                                              
Nitrogen      7.97%    8.15%                                              
______________________________________
EXAMPLE 86
A mixture of 3.14 parts of 2,2,6,6-tetramethylpiperidin-4-ol and 3.50 parts of acetic anhydride was heated on a steam bath for one hour. After this time 20 parts of water were added and heating continued for a further one hour. The solution was carefully neutralised with a saturated solution of sodium bi-carbonate and then ether extracted. The combined ether extracts were washed twice with 5% sodium bi-carbonate solution and twice with brine, the ether solution was then dried over anhydrous magnesium sulphate and the ether removed by distillation under reduced pressure to yield 1-acetyl-2,2,6,6-tetramethylpiperidinyl-4-acetate having a melting point of 33°-4° C. and the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
                   (for                                                   
            Found  C.sub.13 H.sub.23 NO.sub.3)                            
______________________________________                                    
Carbon        64.51%   64.73%                                             
Hydrogen      9.69%    9.54%                                              
Nitrogen      5.67%    5.81%                                              
______________________________________
EXAMPLE 87
A mixture of 15.70 parts of 2,2,6,6-tetramethylpiperidin-4-ol, 22.80 parts of methyl isocyanate and 0.5 parts of 1,4-diazabicyclo[2,2,2]octane in 100 parts of dry benzene was heated under reflux conditions for 24 hours. The benzene solvent was removed by distillation under reduced pressure and 150 parts of water added to the residue which was stood overnight at room temperature. The solid formed was collected by filtration and dried to yield 19.60 parts of a white crystalline solid having a melting point of 167°-8° C. This solid was shown to contain 80% of 4-methylcarbamoyl-1-methylcarbamoyl-2,2,6,6-tetramethylpiperidine from microanalysis and nuclear magnetic resonance spectra.
EXAMPLE 88
a. 2.65 parts of acrylonitrile was added dropwise with stirring to a solution of 8.55 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol and 0.30 parts of 40% potassium hydroxide solution in 80 parts of benzene. Stirring was continued at room temperature for 16 hours after which time the solution was washed with water, dried and the benzene solvent removed by distillation under reduced pressure. Fractional distillation of the residue, under reduced pressure gave 1.70 parts of 4-(2'-cyanoethoxy)-1,2,2,6,6-pentamethylpiperidine having a boiling point of 105°-6° C. at 0.1 mm of Hg and the following elemental analysis by weight:
______________________________________                                    
                  Required                                                
            Found (for C.sub.13 H.sub.24 N.sub.2 O)                       
______________________________________                                    
Carbon        69.27%  69.60%                                              
Hydrogen      10.69%  10.78%                                              
Nitrogen      12.40%   12.49%.                                            
______________________________________
b. To 51 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol a solution of metallic sodium in two parts of tert.butanol was added. 52.5 parts of acrylonitrile was dropped in with rapid stirring. After standing for two days at room temperature the mixture was heated to 80° C. for two hours and distilled under reduced pressure yielding 4-(2'-cyanoethoxy) 1,2,2,6,6-pentamethylpipeidine with a boiling point of 172°-4° C. at 17 mm Hg. This sample was identical to that prepared under Example 88a.
EXAMPLE 89
A misture of 13.0 parts of 4-dodecyloxy-2,2,6,6-tetramethylpiperidine and 3.42 parts of benzyl bromide was heated at 100° C. for 48 hours. Petroleum ether (b.p. 40°-60° C.) was added to the cooled reaction mixture and the 4-dodecyloxy-2,2,6,6-tetramethylpiperidine hydrobromide formed during the reaction was filtered off. The petroleum ether solvent was removed by distillation under reduced pressure and the residue fractionally distilled to give 4-dodecyloxy-1-benzyl-2,2,6,6,-tetramethylpiperidine having a boiling point of 200° C. at 0.5 m.m. of Hg. and the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.28 H.sub.50 NO)                             
______________________________________                                    
Carbon        80.67%   80.90%                                             
Hydrogen      11.82%   11.88%                                             
Nitrogen      3.34%    3.37%                                              
______________________________________
EXAMPLE 90
A mixture of 4-benzyloxy-2,2,6,6,-tetramethylpiperidine and 1.67 parts of ethyl α-bromoacetate in 30 parts of ethyl alcohol was heated under reflux conditions for 115 hours. The ethyl alcohol solvent was removed by distillation under reduced pressure and the residue fractionally distilled to give 4-benzyloxy-1-ethoxycarbonylmethyl-2,2,6,6-tetramethylpiperidine having a boiling point of 145°-6° C. at 0.2 m.m. of Hg. and the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.20 H.sub.31 NO.sub.3)                       
______________________________________                                    
Carbon        71.62%   72.04%                                             
Hydrogen      8.90%    9.37%                                              
Nitrogen      3.94%    4.20%                                              
______________________________________
EXAMPLE 91
A mixture of 25.7 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol and 3.09 parts of boric acid in 100 parts of toluene was heated under reflux conditions with azeotropic removal of water for 24 hours. The toluene solvent was removed by distillation under reduced pressure to give tris-(1,2,2,6,6-pentamethyl-4-piperidinyl)borate having a melting point of 83°-9° C. and the following elemental analysis by weight:
______________________________________                                    
                  Required                                                
           Found  (for C.sub.30 H.sub.20 N.sub.3 O.sub.3 B)               
______________________________________                                    
Carbon       68.85%   69.05%                                              
Hydrogen     11.68%   11.59%                                              
Nitrogen     7.76%    8.06%                                               
______________________________________
EXAMPLE 92
30 parts of 1,2,2,6,6,-pentamethylpiperidin-4-ol were dissolved in 250 parts of sodium added. The solution was heated overnight at reflux temperature and then cooled. 38 parts of 2-phenoxyethanol tosylate were added dropwise and the solution heated at reflux for 5 hours. On cooling the precipitate was filtered off and the filtrate evaporated in vacuo Treatment of the residue with dilute hydrochloric acid and then basification with dilute sodium hydroxide to a pH 10 was followed by extraction with ether. Evaporation afforded a pale yellow oil which was chromatographed on aluminum to give 4-(2'-phenoxyethoxy)-1,2,2,6,6-pentamethylpiperidine as a colourless oil which gave the following elemental analysis by weight:
______________________________________                                    
                   Required                                               
            Found  (for C.sub.18 H.sub.29 NO.sub.2)                       
______________________________________                                    
Carbon        72.49%   74.18%                                             
Hydrogen      9.89%    10.03%                                             
Nitrogen      4.91%    4.81%                                              
______________________________________
EXAMPLE 93
A mixture of 9.87 parts of 4-allyloxy-2,2,6,6-tetramethylpiperidine and 3.03 parts of allyl bromide was heated at 90° C. for 96 hours. Ether was added to the cooled reaction mixture and the 4-allyloxy-2,2,6,6-tetramethylpiperidine hydrobromide formed during the reaction was filtered off. The ether solvent was removed by distillation under reduced pressure and the residue purified by chromatography to give 4-allyloxy-1-allyl-2,2,6,6-tetramethylpiperidine.
EXAMPLES 94-116 Testing in polypropylene film
38 parts of polypropylene were homogenised with 0.076 parts of n-octadecyl-β(4'-hydroxy-3',5'-t-butylphenyl) propionate in a kneading machine over a period of 3 minutes at 200° C. 0.19 parts of the product of Example 13 was then added and homogenisation continued for another 7 minutes.
This composition was compression moulded into films of 0.1 mm thickness at 260° C. for 6 minutes and the films so obtained were then quenched in cold water.
A section measuring 44×100 mm was separated from the 0.1 mm annealed polypropylene foil and exposed to light irradiation in a fademeter device consisting of a circular bank of 28 alternate sunlight and blacklight lamps. The sunlight lamps were 2 feet long, 20-watt fluorescent lamps characterised by a peak emission of 3,100 Angstrom units; the blacklight lamps were 2 feet long, 20-watt ultraviolet lamps characterised by a peak emission of 3,500 Angstrom units. The sample was rotated concentrically about the bank of lamps so that the radiation therefrom was uniformly distributed over the section under test.
The exposed sample was examined periodically and portions of it tested for the percent/elongation at break, the time at which the sample reached 50% of the initial elongation at break was noted.
Similar tests were carried out on polypropylene samples containing, respectively, no stabiliser and known stabilisers, and also stabilisers falling within the scope of German Patent Specification No. 1,929,928. The results obtained are set out in the following table:
                                  TABLE                                   
__________________________________________________________________________
                                          Factor                          
                                          Time to 50% of initial          
                                          elongation at break             
                                          (additive)                      
Example                                   Time to 50% of initial          
Additive                                                                  
     (control)                            elongation at                   
__________________________________________________________________________
                                          break                           
--   none                                 1.0                             
--   2-(2'-hydroxy-3',5'-di-t-butylphenyl)-5-chlorobenzotriazole          
                                          3.2                             
--   4-phenylcarbamoyloxy-2,2,6,6-tetramethylpiperidine                   
                                          1.8                             
--   1,6-bis[4'-carbamoyloxy-2',2',6',6'-tetramethylpiperidine]hexane     
                                          2.4                             
--   2,2,6,6-tetramethylpiperidinyl-4-benzoate                            
                                          2.6                             
--   bis(2,2,6,6-tetramethyl-4-piperidinyl)sebacate                       
                                          4.7                             
 94  1,2,2,6,6-pentamethylpiperidinyl-4-phenylacetate                     
                                          5.2                             
 95  bis(1,2,2,6,6-pentamethyl-4-piperidinyl)terephthalate                
                                          5.3                             
 96  1,2,2,6,6-pentamethylpiperidinyl-4-(p-methoxybenzoate                
                                          5.3                             
 97  1,2,2,6,6-pentamethylpiperidinyl-4-(1'-naphthoate)                   
                                          5.4                             
 98  1,2,2,6,6-pentamethylpiperidinyl-4-octanoate                         
                                          6.2                             
 99  1,2,2,6,6-pentamethylpiperidinyl-4-isobutyrate                       
                                          6.2                             
100  bis(1,2,2,6,6-pentamethyl-4-piperidinyl)sebacate                     
                                          8.0                             
101  2,4-bis(4'-carbamoyloxy-1',2',2',6',6'-pentamethylpiperidine)toluene 
                                          5.2                             
102  4-p-tolylcarbamoyloxy-1,2,2,6,6-pentamethylpiperidine                
                                          5.2                             
103  4-allylcarbamoyloxy-1,2,2,6,6-pentamethylpiperidine                  
                                          5.5                             
104  4-phenylcarbamoyloxy-1,2,2,6,6-pentamethylpiperidine                 
                                          5.6                             
105  4-methylcarbamoyloxy-1,2,2,6,6-pentamethylpiperidine                 
                                          5.8                             
106  1,6-bis[4'-carbamoyloxy-1',2',2',6',6'-pentamethylpiperidine]hexane  
                                          9.2                             
107  bis(1-benzyl-2,2,6,6-tetramethyl-4-piperidinyl)sebacate              
                                          5.0                             
108  1-ethoxycarbonylmethyl-2,2,6,6-tetramethylpiperidinyl-4-(p-methoxyben
     zoate)                               5.1                             
109  1-benzyl-2,2,6,6-tetramethylpiperidinyl-4-(2'-ethylhexanoate)        
                                          5.2                             
110  1-(n-dodecyl)-2,2,6,6-tetramethylpiperidinyl-4-octanoate             
                                          5.2                             
111  1(2'-hydroxyethyl)-2,2,6,6,-tetramethylpiperidinyl-4-octanoate       
                                          5.8                             
112  1-(n-propyl)-2,2,6,6-tetramethylpiperidinyl-4-octanoate              
                                          6.0                             
113  4-(n-dodecyloxy)-1,2,2,6,6-pentamethylpiperidine                     
                                          5.5                             
114  4-(2'-cyanoethoxy)-1,2,2,6,6-pentamethylpiperidine                   
                                          >6.0                            
115  1,4-bis(1',2',2',6',6'-pentamethyl-4'-piperidinyloxy)butane          
                                          >6.0                            
116  Tris(1,2,2,6,6-pentamethyl-4-piperidinyl)borate                      
                                          5.0                             
__________________________________________________________________________
EXAMPLES 117 to 119
The procedure described in Examples 94-116 was repeated except that 0.25% by weight of the light stabiliser under test was used, and, instead of polypropylene, a low-density polyethylene was employed as substrate.
The pressing was conducted at 180° C. and the pressings were compression-moulded into 1 mm. thick plaques at 150° C.
The plaques were stored at 20° C. and were periodically examined visually for the first sign of exudation.
The results obtained are summarised in the following Table which also includes data relating to comparative experiments (known light stabilisers added).
              TABLE                                                       
______________________________________                                    
                             Time                                         
                            to exudation                                  
Example Light stabiliser added                                            
                            (days)                                        
______________________________________                                    
--      2,2,6,6-tetramethylpiperidinyl-                                   
                             15                                           
        4-stearate                                                        
--      bis(2,2,6,6-tetramethyl-4-                                        
                             20                                           
        piperidinyl)sebacate                                              
--      4-stearylcarbamoyloxy-2,2,6,6-                                    
                             13                                           
        tetramethylpiperidine                                             
117     1,2,2,6,6-pentamethylpiperidinyl-                                 
                            >50                                           
        4-stearate                                                        
118     bis(1,2,2,6,6-pentamethyl-4-                                      
                            >50                                           
        piperidinyl(sebacate                                              
119     4-stearylcarbamoyloxy-1,2,2,6,6-                                  
                            >50                                           
        pentamethylpiperidine                                             
______________________________________
EXAMPLES 120 to 122
The procedure described in Examples 117 to 119 was repeated except that the compression moulding was carried out at 200° C. and the substrate used was high-density polyethylene.
The results obtained are set out in the following Table, which also contains data relating to comparative experiments (using a known light stabiliser).
              TABLE                                                       
______________________________________                                    
                              Time                                        
                              to exudation                                
Example                                                                   
       Light Stabiliser       (days)                                      
______________________________________                                    
--     2,2,6,6-tetramethylpiperidinyl-4-                                  
                               10                                         
       stearate                                                           
120    1,2,2,6,6-pentamethylpiperidinyl-                                  
                              >75                                         
       4-stearate                                                         
121    4-stearylcarbamoyloxy-1,2,2,6,6-                                   
                              >75                                         
       .[.tetramethyl.].piperidine                                        
122    I-(n-dodecyl)-2,2,6,6-.[.tetramethyl.].  pentamethylene            
                              >75                                         
       piperidinyl-4-octanoate                                            
______________________________________
EXAMPLES 123 to 128
100 Parts of crystal polystyrene pellets were dry blended with 0.25 part of 1,2,2,6,6-pentamethylpiperidinyl-4-stearate, and the dry blend was homogenised by .[.extension.]. .Iadd.extrusion.Iaddend.. The stabilised pellets so obtained were injection moulded to form plaques 2 mm. thick. These plaques were exposed for 3000 hours in a "Xenotest 150" exposure unit, and any yellowing of the plaques was measured by determining the yellowness factor by means of the following equation: ##EQU1## wherein the Δ T values represent the transmission loss of the sample at wavelength of 420 .[.m.]..Iadd.n.Iaddend.m. and 680 .[.m.]..Iadd.n.Iaddend.m. respectively, after exposure in the Xenotest unit, the T.sub.(560) represents the transmission value of an unexpected sample at a wavelength of 560 .[.m.]..Iadd.n.Iaddend.m.
The results obtained, as well as the results relating to a control experiment and other compositions of this invention are recording in the following Table.
              TABLE                                                       
______________________________________                                    
                             Yellowing                                    
                             factor after                                 
Example                                                                   
       Light Stabiliser      3000 hours                                   
______________________________________                                    
--     none                  35.0                                         
123    1,2,2,6,6-pentamethylpiperidinyl-                                  
                             10.0                                         
       4-stearate                                                         
124    1-benzyl-2,2,6,6-tetramethylpiperi-                                
                             9.8                                          
       dinyl-4-(2'-ethylhexanoate)                                        
125    1,2,2,6,6-pentamethylpiperidinyl-                                  
                             9.5                                          
       4-(n-octanoate)                                                    
126    4-(2'-cyanoethoxy)-1,2,2,6,6-penta-                                
                             8.0                                          
       methylpiperidine                                                   
127    4-stearylcarbamoyloxy-1,2,2,6,6-                                   
                             7.5                                          
       pentamethylpiperidine                                              
128    bis-(1,2,2,6,6-pnetamethyl-4-                                      
                             6.6                                          
       piperidinyl)sebacate                                               
______________________________________
EXAMPLES 129 To 132
25 parts by weight of a polyester-based film-forming polyurethane were dissolved in 75 parts by weight of a 1:1 mixture (by volume) of dimethylformamide and acetone, and 1% by weight of 4(2'-cyanoethoxy)-1,2,2,6,6-pentamethylpiperidine was added.
The clear and homogeneous solution was drawn out on a glass plate to a film of 400-500μ thickness, which was then dried as follows:
at 50° C. for 4 minutes
at 140° C. for 6 minutes
The final thickness of the film was 80-100μ.
The dried film samples were removed from the glass plate, mounted on white cardboard and exposed in a "Xenotest 450" exposure unit, one half of the exposed sample being covered to facilitate subsequent visual estimation of yellowing due to exposure. The sample was controlled and rated visually at intervals of 100 hours.
The data obtained are set out in the following Table which also includes data relating to a control experiment (no added light stabiliser) and to other experiments using stabilisers of this invention.
              TABLE                                                       
______________________________________                                    
                          Time to onset of                                
Example Light Stabiliser  yellowing (hours)                               
______________________________________                                    
--      none              <100                                            
129     4-(2'-cyanoethoxy)-1,2,2,6,6-                                     
                          200                                             
        pentamethylpiperidine                                             
130     1,2,2,6,6-pentamethyl-                                            
                          300                                             
        piperidinyl-4-octanoate                                           
131     bis-(1,2,2,6,6-pentamethyl-                                       
                          300                                             
        4-piperidinyl)sebacate                                            
132     4-phenylcarbamoyloxy-1-n-                                         
                          400                                             
        propyl-2,2,6,6-tetramethyl-                                       
        piperidine                                                        
______________________________________
EXAMPLES 133-135
1000 Parts by weight of unstabilised polypropylene powder were thoroughly dry-blended with 1 part by weight of n-octadecyl-β-(4'-hydroxy-3',5'-di-t-butylphenyl) propionate and 2 parts by weight of 1,2,2,6,6-pentamethyl-4-piperidinyl-(3',5'-di-t-butyl-4'-hydroxy) benzoate. The dry-blend was extruded at cylinder temperatures of from 180° to 220° C., and the resulting strand was granulated. The stabilised formulation so obtained was melt-spun and stretched under the following conditions:
______________________________________                                    
Extruder temperatures 230/265/275° C.                              
Melt temperatures at the dye                                              
                      270° C.                                      
Spinning speed        400 m./minute                                       
Stretching Ratio      1:5                                                 
Titer of Multifilament                                                    
                      130/137 denier                                      
Tensile Strength      6 g./denier                                         
______________________________________
The multifilament obtained was mounted on a sample holder of Xenotest 150 apparatus (Quarzlampen GmbH) using white cardboard as backing. In intervals of 200 hours of exposure time, 5 fiber samples are measured for their retained tensile strength. The data obtained are plotted against exposure time and the exposure time (T) to give 50% loss or original tensile strength is derived from graph. This value is taken as the failure time.
              TABLE                                                       
______________________________________                                    
                           Time (T)                                       
Ex-                        to 50%   Factor                                
am-                        retained T                                     
ple                        tensile  stabiliser                            
No.  Light Stabiliser      strength T control                             
______________________________________                                    
none none                    430    1.0                                   
     2-(2'-hydroxy-3',5'-di-t-butylphenyl)-                               
                             530    1.2                                   
     5-chlorobenzotriazole                                                
133  1,2,2,6,6-Pentamethyl-4-piperidinyl-                                 
                           1,400    3.3                                   
     (3',5'-di-t-butyl-4'-hydroxy                                         
     benzoate)                                                            
134  1,2,2,6,6-Pentamethyl-4-piperidinyl-β-                          
                           1,600    3.7                                   
     (3',5'-di-t-butyl-4'-hydroxyphenyl)                                  
     propionate                                                           
135  Bis(1,2,2,6,6-pentamethyl-4-                                         
                           2,600    6.0                                   
     piperidinyl)sebacate                                                 
______________________________________
EXAMPLES 136 to 144
The procedure described in Examples 94 to 116 was repeated except that the annealed polypropylene specimens were exposed to light irradiation in a Xenotest 450 exposure unit rather than in the fademeter device.
The result obtained are summarised in the following Table which also includes data relating to a control experiment (no added light stabiliser) and a comparative experiment (a known light stabiliser added).
              TABLE                                                       
______________________________________                                    
                                 Time                                     
                                 to                                       
Ex-                              Failure                                  
ample  Light Stabiliser          (hours)                                  
______________________________________                                    
--     none (control)            800                                      
--     2-(2'-hydroxy-3',5'-di-t-butylphenyl)-                             
                                 1630                                     
       5-chlorobenzotriazole                                              
136    bis(1,2,2,6,6-pentamethyl-4-                                       
                                 >9000                                    
       piperidinyl)sebacate                                               
137    1,2,2,6,6-pentamethylpiperidinyl-4-                                
                                 10,000                                   
       β-(3',5'-di-t-butyl-4'-hydroxyphenyl)                         
       propionate                                                         
138    1,2,2,6,6-pentamethylpiperidinyl-4-                                
                                 >8600                                    
       (3',5'-di-t-butyl-4'-hydroxy benzoate)                             
139    1,2,2,6,6-pentamethylpiperidinyl-4-                                
                                 6500                                     
       octanoate                                                          
140    4-phenylcarbamoyloxy-1,2,2,6,6-pentamethyl                         
                                 >7000                                    
       piperidine                                                         
141    4-methylcarbamoyloxy-1,2,2,6,6-                                    
                                 6000                                     
       pentamethylpiperidine                                              
142    1,2,2,6,6-pentamethylpiperidinyl-4-                                
                                 >6000                                    
       cyclohexane-carboxylate                                            
143    1,2,2,6,6-pentamethylpiperidinyl-4-                                
                                 >6000                                    
       stearate                                                           
144    1,2,2,6,6-pentamethylpiperidinyl-4-                                
                                 >5000                                    
       benzoate                                                           
______________________________________
EXAMPLES 145-150
100 Parts by weight of polyamide-6 pellets containing 1.8 parts by weight of TiO2 were dry-blended with 0.5 part of 4-benzyloxy-1,2,2,6,6-pentamethyl piperidine. The resulting mixture was melt-spun directly into monofilaments of 20 denier. The monofilaments were mounted on white cardboard without tension and were exposed to light radiation in a Xenotest 450 exposure unit.
After 500, 1,000, 1,500 and 2000 hours of exposure time respectively, 5 fiber samples of each formulation and time interval were tested for tensile strength. The arithmetic mean percentage values of residual tensile strength were plotted as a function of exposure time. The failure points - time to 50% loss of original tensile strength--were obtained from these graphs.
              TABLE                                                       
______________________________________                                    
                            Time to 50% loss                              
                            of original ten-                              
Ex-                         sile strength                                 
ample Light Stabiliser      (hours)                                       
______________________________________                                    
--    none (control)         475                                          
145   4-benzyloxy-1,2,2,6,6-penta-                                        
                            1420                                          
      methylpiperidine                                                    
146   bis(1,2,2,6,6-pentamethyl-4-                                        
                            1600                                          
      piperidinyl)sebacate                                                
147   1,2,2,6,6-pentamethylpiperi-                                        
                            1450                                          
      dinyl-4-octanoate                                                   
148   .[.1.].  4 -phenylcarbamoyloxy-1,2,2,6,6-                           
                            1450                                          
      pentamethylpiperidine                                               
149   1,6-bis[4'-carbamoyloxy-1',2'-                                      
                            1500                                          
      2',6',6'-pentamethylpiperidine)                                     
      hexane                                                              
150   1,4-bis[1',2',2',2',6',6'-penta-                                    
                            1600                                          
      methyl-4'-piperidinyloxy)butane                                     
______________________________________

Claims (6)

What we claim is:
1. A compound having the formula: ##STR160## wherein .[.R111 and RIV are the same or different and each is a straight or branched alkyl group having from 1 to 12 carbon atoms or RIII and RIV together with the carbon atom to which they are each attached from a cycloalkyl group having from 5 to 12 carbon atoms,.]. Y is a straight- or branched alkyl group having from 1 to 12 carbon atoms, an alkenyl group having from 3 to 12 carbon atoms or an aralkyl group having from 7 to 12 carbon atoms and .Iadd.when q is 1, .Iaddend.R12 is hydrogen or .Iadd.when q is 1 or 2, R12 is .Iaddend.a saturated or unsaturated hydrocarbyl group containing up to 20 carbon atoms optionally substituted.[., Y.]. .Iadd.by .Iaddend.halogen or alkoxy having from 1 to 4 carbon atoms and q is .Iadd.1 or .Iaddend.2 and a salt thereof selected from a phosphate, carbonate, sulfate, chloride, acetate, stearate, maleate, citrate, .[.tertrate.]. .Iadd.tartrate, .Iaddend..[.oxolate.]. .Iadd.oxalate, .Iaddend.benzoate and substituted carbamate.
2. A compound as claimed in claim 1 wherein R12 is an aliphatic group having from 1 to 20 carbon atoms, an alicyclic group having from 5 to 15 carbon atoms or an aromatic group having from 6 to 15 carbon atoms.
3. A compound as claimed in claim 2 wherein R12, when q is 1, is methyl, ethyl, propyl, isopropyl, n-.Iadd.butyl, 2-ethylhexyl, dodecyl, octadecyl, allyl, oleyl, cyclohexyl, benzyl, phenyl, 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 2,4-dimethylphenyl, 2,6-dimethylphenyl, naphth-1-yl or naphth-2-yl; or when q is 2, .Iaddend.is .[.a.]. 1,2-ethylene, 1,6-hexylene, 2,4,4-trimethyl-1,6-hexylene, 1,3-.Iadd.phenylene, .Iaddend..[.or.]. 1,4-phenylene, 2,4-tolyene, 1,5-naphthylene or 4,4'-diphenylmethylene .[.group.]..
4. A compound as claimed in claim 1 wherein .[.Y1 .]. .Iadd.Y .Iaddend.is methyl.
5. A compound as claimed in claim 1 in the form of its salt of an inorganic or organic acid. .[.6. A compound of formula IV as defined in claim 1
wherein RIII and RIV are methyl..]. 7. A compound according to claim 1 which is 1,6-bis-(4'-carbamoyloxy-1',2',6',6'-pentamethylpiperidine)hexane. .Iadd. 8. A compound according to claim 1 which is 4-phenylcarbamoyloxy-1,2,2,6,6-pentamethylpiperidine. .Iaddend..Iadd. 9. A compound as defined in claim 1 where Y is methyl and R12, when q is 1, is alkyl of up to 20 carbon atoms, alkenyl of up to 20 carbon atoms, cycloalkyl of 5 to 12 carbon atoms, aryl of 6 to 12 carbon atoms or aralkyl of 7 to 9 carbon atoms, or, when q is 2, is alkylene of up to 20 carbon atoms, alkenylene of up to 20 carbon atoms, cycloalkylene of 5 to 12 carbon atoms or arylene of 6 to 12 carbon atoms. .Iaddend..Iadd. 10. A compound is claimed in claim 1 wherein Y is methyl and R12, when q is 1, is methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, t-butyl, n-pentyl, 2-ethylpropyl, 2-methylbutyl, n-hexyl, 2-methylpentyl, n-heptyl, 2-ethylpentyl, n-octyl, 2-ethylhexyl, 2,2,4-trimethylpentyl, n-decyl, n-dodecyl, n-tetradecyl, n-octadecyl, eicosyl, mesityl, allyl, oleyl, cyclopentyl, cyclohexyl, methylcyclohexyl, t-butylcyclohexyl, t-octylcyclohexyl, cyclodedecyl, 1-perhydronaphthyl, 2-perhydronaphthyl, adamantyl, cyclopentylmethyl, cyclohexylmethyl, 2-cyclohexylethyl, benzyl, 2-phenylethyl, naphth-1-ylmethyl, naphth-2-ylmethyl, 2-(naphth-1-yl)ethyl, 2-(naphth-2-yl)ethyl, phenyl, 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 2,4-dimethylphenyl, 2,6-dimethylphenyl, 4-chlorophenyl, 3-chloro-4-methylphenyl, 2-ethylphenyl, 4-t-butylphenyl, 2,3-dichlorophenyl, 2,5-dichlorophenyl, naphth-1-yl, naphth-2-yl or biphenylyl; or, when q is 2, is methylene, 1,2- ethylene, 1,4-n-butylene, 1,6-n-hexylene, 1,8-n-octylene, 2,4,4-trimethyl-1,6-hexylene, 1,10-n-decylene, 1,2-eicosylene, 1,2-eicosenylene, 1,3-cyclohexylene, 1,4-cyclohexylene, 1,3-phenylene, 1,4-phenylene, 2,4-tolylene, 1,5-naphthylene, 4,4'-diphenylene, 4,4'-diphenylmethylene, 3,3'-dimethyl-4,4'-diphenylene, or 3,3'-dimethyl-4,4'-diphenylmethylene. .Iaddend.
US05/938,849 1971-11-30 1978-09-01 Piperidine derivatives Expired - Lifetime USRE31343E (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
GB5548771 1971-11-30
GB55487/71 1971-11-30
GB2845872*[A GB1399239A (en) 1971-11-30 1972-06-17 Piperidine derivatives
GB28458/72 1972-06-17
GB35473/72 1972-06-28
GB3547372 1972-07-28

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
US31003172A Continuation 1971-11-30 1972-11-28
US05/577,502 Reissue US4021432A (en) 1971-11-30 1975-05-14 Piperidine derivatives

Publications (1)

Publication Number Publication Date
USRE31343E true USRE31343E (en) 1983-08-09

Family

ID=27258723

Family Applications (2)

Application Number Title Priority Date Filing Date
US05/938,849 Expired - Lifetime USRE31343E (en) 1971-11-30 1978-09-01 Piperidine derivatives
US05/938,974 Expired - Lifetime USRE31342E (en) 1971-11-30 1978-09-01 Piperidyl carboxylates

Family Applications After (1)

Application Number Title Priority Date Filing Date
US05/938,974 Expired - Lifetime USRE31342E (en) 1971-11-30 1978-09-01 Piperidyl carboxylates

Country Status (21)

Country Link
US (2) USRE31343E (en)
JP (1) JPS5920709B2 (en)
AT (1) AT324009B (en)
BE (1) BE792043A (en)
CA (1) CA997767A (en)
CH (2) CH586252A5 (en)
CS (1) CS190377B2 (en)
DD (1) DD106190A5 (en)
DE (2) DE2258752A1 (en)
ES (1) ES409079A1 (en)
FR (3) FR2182789B1 (en)
GB (1) GB1399239A (en)
HK (1) HK47877A (en)
HU (1) HU167244B (en)
IL (1) IL40888A (en)
IT (1) IT971346B (en)
MY (1) MY7800025A (en)
NL (1) NL174942C (en)
RO (2) RO64573A (en)
SE (1) SE454277B (en)
SU (1) SU584795A3 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4925888A (en) 1987-10-21 1990-05-15 Basf Aktiengesellschaft Mixture for stabilizing polyurethanes
US20160176855A1 (en) * 2013-07-30 2016-06-23 Clariant International Ltd. Novel Sterically Hindered Cyclic Amines
US10487193B2 (en) * 2015-01-07 2019-11-26 Clariant Plastics & Coatings Ltd Stabilization of polyamides

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1402888A (en) * 1972-10-21 1975-08-13 Ciba Geigy Ag Piperidine derivatives
CH589056A5 (en) * 1973-12-10 1977-06-30 Ciba Geigy Ag
JPS51132242A (en) * 1975-03-22 1976-11-17 Adeka Argus Chem Co Ltd Light stabilising composition for synthetic resin
DE2627688A1 (en) * 1975-06-30 1977-01-27 Ciba Geigy Ag DISABLED PIPERIDINE CARBONIC ACIDS, METAL SALTS THEREOF AND THEREFORE STABILIZED POLYMERS
DE2718458A1 (en) * 1976-05-04 1977-11-24 Ciba Geigy Ag NEW STABILIZERS
DE2805838A1 (en) * 1977-02-24 1978-08-31 Ciba Geigy Ag NEW 4-ACYLOXYPIPERIDINE
JPS5469162A (en) * 1977-11-15 1979-06-02 Dainichi Seika Kogyo Kk Stabilized urethane polymer
EP0002260B1 (en) * 1977-12-02 1982-07-14 Ciba-Geigy Ag Malonic acid derivatives of sterically hindered piperidines, process for their preparation and stabilised organic matter
JPS559064A (en) * 1978-07-03 1980-01-22 Sankyo Co Ltd Novel stabilizer
ATE4992T1 (en) * 1978-07-25 1983-10-15 Imperial Chemical Industries Plc POLYOLEFIN ARTICLES STERILIZABLE BY GAMMA RADIATION.
US4311820A (en) * 1979-02-14 1982-01-19 Ciba-Geigy Corporation Homopolymers and copolymers of vinyl ethers of polyalkylpiperidinols and their use as stabilizers for plastics
IT7928324A0 (en) * 1979-12-21 1979-12-21 Chimosa Chimica Organica Spa PIPERIDINE DERIVATIVES, STABILIZERS FOR SYNTHETIC POLYMERS.
DE3201415A1 (en) * 1981-01-28 1982-08-26 Sandoz-Patent-GmbH, 7850 Lörrach 4-Aminomethylpolyalkylpiperidines
CS229069B1 (en) * 1981-09-23 1984-05-14 Julius Durmis Composition for stabilizing polymers and method of preparing same
JPS58113236A (en) * 1981-12-28 1983-07-06 Tounen Sekiyu Kagaku Kk Polyolefin composition
US4590268A (en) * 1982-05-10 1986-05-20 Ciba-Geigy Corporation Process for the preparation of 1-diorganocarbamoyl-polyalkylpiperidines
US4569997A (en) * 1982-08-10 1986-02-11 Ciba Geigy Corporation Polyalkylpiperidine compounds
DE3312611A1 (en) * 1983-04-08 1984-10-11 Röhm GmbH, 6100 Darmstadt METHOD FOR PRODUCING UV-PROTECTED MULTILAYERED PLASTIC MOLDED BODIES
DE3345376A1 (en) * 1983-12-15 1985-06-27 Basf Ag, 6700 Ludwigshafen FURAN-3-CARBONSAEUR DERIVATIVES
DE3522678A1 (en) * 1985-06-25 1987-01-08 Basf Ag TETRAHYDROFURANCARBONSAEUR DERIVATIVES
JPS6248745A (en) * 1985-08-28 1987-03-03 Mitsubishi Petrochem Co Ltd Polyolefin composition
IT1189095B (en) * 1986-05-02 1988-01-28 Enichem Sintesi PROCEDURE FOR THE SYNTHESIS OF ALLILATED DERIVATIVES OF 2,2,6,6-TETRALKYLPIPERIDINOLS
IT1191804B (en) * 1986-06-11 1988-03-23 Enichem Sintesi PROCEDURE FOR THE PREPARATION OF N-ALYL-PIPERIDINE DERIVATIVES
DE3724222A1 (en) * 1987-07-22 1989-02-02 Huels Chemische Werke Ag LIGHT STABILIZERS
IT1222647B (en) * 1987-09-11 1990-09-05 Eniricerche Spa AMERICAN COMPOUNDS STERICALLY PREVENTED AND PROCEDURE FOR THEIR PREPARATION
DE58907381D1 (en) * 1988-05-27 1994-05-11 Ciba Geigy Unsaturated derivatives of 2,2,6,6-tetramethylpiperidine.
ES2050274T3 (en) * 1988-06-14 1994-05-16 Ciba Geigy Ag PROCEDURE FOR THE PHOTOCHEMICAL STABILIZATION OF UNDYED AND DYED POLYPROPYLENE FIBERS.
US4927898A (en) * 1988-09-06 1990-05-22 Union Carbide Chemicals And Plastics Company Inc. Polysiloxanes with sterically hindered heterocyclic moiety
DE3844356A1 (en) * 1988-12-30 1990-07-05 Basf Ag 4- (2'-ETHYLHEXANOYLOXY) -2,2,6,6-TETRAMETHYL PIPERIDINE
GB9023023D0 (en) * 1990-10-23 1990-12-05 Barlow Richard B Pharmaceutical compositions
US5180830A (en) * 1991-04-24 1993-01-19 Himont Incorporated Process for preparing hindered amine light stabilizers
NL9101619A (en) * 1991-09-25 1993-04-16 Harcros Chemicals Bv STABILIZERS FOR ORGANIC MATERIALS.
US5169949A (en) * 1991-09-30 1992-12-08 Himont Incorporated Monomeric hindered amine esters of monocarboxylic resin acid having 20 carbon atoms
AU7216796A (en) * 1995-10-12 1997-04-30 Ciba-Geigy Ag Thermally stable hindered amines as stabilizers
EP1184442A1 (en) * 2000-08-30 2002-03-06 Clariant International Ltd. Liquid crystal mixture
US6727300B2 (en) 2000-11-03 2004-04-27 Cytec Technology Corp. Polymeric articles containing hindered amine light stabilizers based on multi-functional carbonyl compounds
US6545156B1 (en) * 2000-11-03 2003-04-08 Cytec Technology Corp. Oligomeric hindered amine light stabilizers based on multi-functional carbonyl compounds and methods of making same
US6492521B2 (en) 2000-11-03 2002-12-10 Cytec Technology Corp. Hindered amine light stabilizers based on multi-functional carbonyl compounds and methods of making same
US6414155B1 (en) 2000-11-03 2002-07-02 Cytec Technology Corp. Oligomeric hindered amine light stabilizers based on multi-functional carbonyl compounds and methods of making same
US6525131B1 (en) 2001-09-18 2003-02-25 Crompton Corporation Aromatic diamine polyurethane curatives with improved stability
EP1444222A1 (en) * 2001-10-23 2004-08-11 Council Of Scientific And Industrial Research Tinuvin p-hindred amine light stabilizer and derivatives thereof, and a process for the preparation thereof
US6492518B1 (en) 2001-10-30 2002-12-10 Council Of Scientific And Industrial Research Tinuvin P-hindred amine light stabilizer and derivatives thereof
JP5283153B2 (en) 2007-10-25 2013-09-04 株式会社Ａｄｅｋａ Synthetic resin composition and automotive interior / exterior material
KR101602750B1 (en) 2008-03-10 2016-03-11 가부시키가이샤 아데카 Synthetic resin composition, and automotive interior/exterior material comprising the same
JP5656213B2 (en) * 2010-01-19 2015-01-21 日本化薬株式会社 Carboxylic acid composition and curable resin composition containing the carboxylic acid composition
MX2016000313A (en) * 2013-07-08 2016-08-08 Basf Se Novel light stabilizers.
WO2015177193A1 (en) * 2014-05-21 2015-11-26 Solvay Specialty Polymers Usa, Llc Stabilizer compounds

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2746964A (en) * 1953-11-02 1956-05-22 Lakeside Lab Inc Dicarboxylic acid esters of nu-alkyl-3-hydroxypiperidine and salts thereof
US3120540A (en) * 1961-09-25 1964-02-04 Warner Lambert Pharmaccutical Bis (polymethyl)-4-piperidinol alkanoates
US3640928A (en) * 1968-06-12 1972-02-08 Sankyo Co Stabilization of synthetic polymers
US3840494A (en) * 1971-01-29 1974-10-08 Sankyo Co Process for preparing acid esters of 4-piperidinol derivatives and their use as stabilizers
US4021432A (en) * 1971-11-30 1977-05-03 Ciba-Geigy Corporation Piperidine derivatives

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3705166A (en) * 1969-08-15 1972-12-05 Sankyo Co Acrylic acid derivatives of 2,2,6,6-tetramethylpiperidines
US4049647A (en) * 1971-11-30 1977-09-20 Ciba-Geigy Corporation Bis piperidyl carboxylates

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2746964A (en) * 1953-11-02 1956-05-22 Lakeside Lab Inc Dicarboxylic acid esters of nu-alkyl-3-hydroxypiperidine and salts thereof
US3120540A (en) * 1961-09-25 1964-02-04 Warner Lambert Pharmaccutical Bis (polymethyl)-4-piperidinol alkanoates
US3640928A (en) * 1968-06-12 1972-02-08 Sankyo Co Stabilization of synthetic polymers
US3840494A (en) * 1971-01-29 1974-10-08 Sankyo Co Process for preparing acid esters of 4-piperidinol derivatives and their use as stabilizers
US4021432A (en) * 1971-11-30 1977-05-03 Ciba-Geigy Corporation Piperidine derivatives

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4925888A (en) 1987-10-21 1990-05-15 Basf Aktiengesellschaft Mixture for stabilizing polyurethanes
US20160176855A1 (en) * 2013-07-30 2016-06-23 Clariant International Ltd. Novel Sterically Hindered Cyclic Amines
US10487193B2 (en) * 2015-01-07 2019-11-26 Clariant Plastics & Coatings Ltd Stabilization of polyamides

Also Published As

Publication number Publication date
SU584795A3 (en) 1977-12-15
IT971346B (en) 1974-04-30
CH586252A5 (en) 1977-03-31
CH585714A5 (en) 1977-03-15
JPS4865180A (en) 1973-09-08
AT324009B (en) 1975-08-11
NL174942C (en) 1984-09-03
JPS5920709B2 (en) 1984-05-15
RO64573A (en) 1979-08-15
DD106190A5 (en) 1974-06-05
RO71050A (en) 1981-09-24
NL174942B (en) 1984-04-02
FR2182789A1 (en) 1973-12-14
HK47877A (en) 1977-09-23
DE2258752C2 (en) 1989-10-26
SE454277B (en) 1988-04-18
FR2183293A1 (en) 1973-12-14
CS190377B2 (en) 1979-05-31
IL40888A0 (en) 1973-01-30
HU167244B (en) 1975-09-27
MY7800025A (en) 1978-12-31
USRE31342E (en) 1983-08-09
ES409079A1 (en) 1976-04-16
FR2183294B1 (en) 1978-05-26
FR2183293B1 (en) 1977-07-29
FR2183294A1 (en) 1973-12-14
DE2258752A1 (en) 1973-06-07
FR2182789B1 (en) 1976-01-30
IL40888A (en) 1976-10-31
CA997767A (en) 1976-09-28
NL7216278A (en) 1973-06-04
BE792043A (en) 1973-05-29
GB1399239A (en) 1975-06-25

Similar Documents

Publication Publication Date Title
USRE31343E (en) Piperidine derivatives
US4021432A (en) Piperidine derivatives
US4049647A (en) Bis piperidyl carboxylates
US4046737A (en) Piperidine derivatives
US4038280A (en) Hydroxyaryl-tetramethyl-piperidines
US4014887A (en) Substituted piperidin-4-ols
US5410047A (en) Polymer stabilizers containing both hindered amine and hydroxlamine moieties
US4075165A (en) Stabilization of polymers by penta- or hexa-substituted 4-piperidinol derivatives
US3992390A (en) Esters of piperidinols
US3850877A (en) Piperidine stabilizers for polymers
US4191683A (en) Derivatives of 4-aminopiperidine as stabilizers for polymers
US3939168A (en) 4-Piperidine acetamides
US4028334A (en) Piperidine derivatives
US3937711A (en) 4-(carboxamidoethyl) piperidines
US4972009A (en) Polymer stabilizers containing both hindered amine and nitrone moieties
US4780493A (en) Novel piperidine compounds
US3954779A (en) 4-(4&#39;-Hydroxycyclohexyl)-2,2,6,6-tetramethyl piperidines
US4910238A (en) Poly(2,2,6,6-tetramethyl piperidyl amino)-1,3,5-triazines as stabilizers for synthetic polymer compositions
US3956310A (en) N-carbamoyl imidazolidinones and imidazolidinethiones
US3959291A (en) Piperidine derivatives
US4309546A (en) Piperidino pyrrolidinones
US4377690A (en) Hindered piperidine ligands
IL44629A (en) Stabilization of synthetic polymers by means of certain 1-substituted piperidine derivatives
US4139520A (en) Compositions stabilized with hindered piperidine carboxylic acids or metal salts thereof
US4118368A (en) Synthetic polymer stabilizers