GB918360A - Bis-1,3-dioxolanes - Google Patents

Bis-1,3-dioxolanes

Info

Publication number
GB918360A
GB918360A GB3267961A GB3267961A GB918360A GB 918360 A GB918360 A GB 918360A GB 3267961 A GB3267961 A GB 3267961A GB 3267961 A GB3267961 A GB 3267961A GB 918360 A GB918360 A GB 918360A
Authority
GB
United Kingdom
Prior art keywords
bis
iii
carbon atoms
divinyl
formula
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
Application number
GB3267961A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB918360A publication Critical patent/GB918360A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F24/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/15Heterocyclic compounds having oxygen in the ring
    • C08K5/156Heterocyclic compounds having oxygen in the ring having two oxygen atoms in the ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Paints Or Removers (AREA)

Abstract

Bis-1,3-dioxolanes having the formula <PICT:0918360/III/1> in which R is a tetravalent organic radical having at least 2 carbon atoms, each terminal carbon atom of the radical being a member of one dioxolane ring, and X is an organic radical comprising 2 carbon atoms in the dioxolane ring, at least one of said carbon atoms in X bearing an alkenyl substituent, are used for the production of coating compositions which can be applied and dried at room temperature or for a short time at slightly elevated temperature, e.g. 50 DEG -150 DEG C., to give hard, glossy films. The compounds are usually mixed with metallic driers such as lead, manganese, zinc, iron, nickel, cadmium, copper, tin, zirconium and, preferably, cobalt salts. Suitable salts, for example, are acetates, naphthenates, linoleates, resinates, tallates, oxalates and phthalates. Other additives which may be used as solvents, plasticizers, pigments, extenders, inhibitors and flow-control agents. Other film-forming materials, such as polymers and copolymers of acrylic esters, vinyl acetate and styrene and unsaturated polyesters may also be added to the compositions. Examples are given of the preparation of coating compositions by mixing (a) the compound of formula <PICT:0918360/III/2> with (i) cobalt butyl phthalate solution to give a clear hard film at room temperature in a few days and at 110 DEG C. in 20 mins. and (ii) with titanium dioxide, toluene and cobalt butyl phthalate to give a coating composition which could be sprayed on glass ceramics, wood and metal; (b) a compound of the general formula given above, in which R is <FORM:0918360/III/1> and X is <FORM:0918360/III/2> is mixed with 1% of cobalt butyl phthalate to give a film drying at room temperature in a few days and at 110 DEG C. in 30 mins.; (c) a compound of the general formula given above in which R is <FORM:0918360/III/3> and X is <FORM:0918360/III/4> is mixed with a small amount of cobalt butyl phthalate to give a composition which is used for coating steel panels; (d) bis-(4,5-divinyl-1,3-dioxol-2-yl) benzene is mixed with toluene and cobalt butyl phthalate to give a coating composition for steel panels; and (e) the compound of formula <FORM:0918360/III/5> is mixed with 1% of cobalt butyl phthalate and used as a coating composition for panels.ALSO:The invention comprises bis-1,3-dioxolanes of the formula <FORM:0918360/IV (b)/1> in which R is a tetravalent organic radical having at least 2 carbon atoms, each terminal carbon atom of the radical being a member of one dioxolane ring, and X is an organic radical comprising 2 carbon atoms in the dioxolane ring, at least one of said ring carbon atoms carrying an alkenyl substituent. Preferably the terminal carbon atoms in R carry a hydrogen atom. The compounds may be prepared by reacting at least one alkenyl substituted ethylene glycol of formula HO-X-OH with at least one dialdehyde or diketone of formula O=R=O, or lower alkyl tetraacetals or ketals thereof, at a temperature of 50-150 DEG C. in the presence of an acidic catalyst. Suitable alkenyl substituted glycols are, for example, 1,2-divinyl; 1,2-diisopropenyl-; 1,2-di-(a -isopropylvinyl)-; 1,2 - dipropenyl-; 1,2 - divinyl - 1,2-dimethyl-; 1,2 - dibut - 11 - enyl-; 1,2-dipent-11-enyl-; 1,2-di-(hepta-1,3,5-trienyl)-; 1,2-dihex-11-enyl-; 1,2-dihept-11-enyl-; 1,2-diphenyl-1,2-divinyl-; 1,2 - dithenyl - 1,2 - divinyl-; 1-vinyl-2-thenyl-; 1,2-di-(2-methylpropen-1-yl)-; 1-vinyl-; 1-vinyl-2-cyclohexyl-; 1-isopropenyl-; 1-furyl-2 - vinyl-; and 1,1-divinyl-2-furfuryl-ethylene glycol. Suitable aldehydes, ketones, acetals and ketals are glyoxal; glutaraldehyde; adipaldehyde; terephthaldehyde; 2,5-furan-diol; oxybis-(5-methylene-2-furfuraldehyde); 2,5-furandi-(3-propional); 1,2-di-(6-formyl-2-tetrahydro-pyranoxy)ethane; 2,2-bis[p-6-formyl - 2 - tetrahydropyranoxy)-phenyl]propane; dodecane-1, 12-diol; 1,1,3,3-tetraethoxy propane; 1,1,3-trimethoxy-3-ethoxy propane; suberic dialdehyde tetraethyl acetal; 1,1,4,4-tetraethoxy ethane; 1,1,7,7-tetraethoxy-hept-3,4-ene; 2,2,5,5-tetraethoxyfuran; cyclohexane - 1,6 - dione; acetonyl acetone; 1,3-diphenyl-1,3-propane-dione; 1,4-dimethyl-1,1,4,4-tetraethoxy butane and 1,8-diethyl-1,1,8,8-tetramethoxy octane. Suitable catalysts are, for example, strong mineral acids, which may be deposited on silica-alumina carriers, or organic acids. Stablizers, e.g. hydroquinone or tertiary butyl catechol, may be added to the reaction mixture. Examples are given of the preparation of various of the new compounds and it is stated that bis-[4-(a -chlorovinyl)-5-vinyl-1,3-dioxol-2-yl]methane may be prepared in a similar manner. 2,2 - Bis - [p-(6-formyl-2-tetrahydropyranoxy) phenyl]-propane used as starting material in Example 5 is prepared by reacting 2,2-bis-(41-hydroxyphenyl)propane with bisacrolein.
GB3267961A 1960-09-21 1961-09-12 Bis-1,3-dioxolanes Expired GB918360A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US5738960A 1960-09-21 1960-09-21

Publications (1)

Publication Number Publication Date
GB918360A true GB918360A (en) 1963-02-13

Family

ID=22010284

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3267961A Expired GB918360A (en) 1960-09-21 1961-09-12 Bis-1,3-dioxolanes

Country Status (3)

Country Link
BE (1) BE608042A (en)
GB (1) GB918360A (en)
NL (1) NL269459A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102408332A (en) * 2011-11-14 2012-04-11 无锡英普林纳米科技有限公司 Ultraviolet curing degradable cross-linking monomer and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102408332A (en) * 2011-11-14 2012-04-11 无锡英普林纳米科技有限公司 Ultraviolet curing degradable cross-linking monomer and preparation method thereof

Also Published As

Publication number Publication date
BE608042A (en) 1962-03-11
NL269459A (en) 1964-06-25

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