CA1262136A

CA1262136A - N-(SUBSTITUTED CYCLIC ALKYLENEIMINE)-.alpha.-(3,5-DI- ALKYL-4-HYDROXYPHENYL)-.alpha.',.alpha."-DIALKYL ACETAMIDES

Info

Publication number: CA1262136A
Application number: CA000465952A
Authority: CA
Inventors: John T. Lai; Pyong N. Son
Original assignee: BF Goodrich Corp
Current assignee: Goodrich Corp
Priority date: 1983-11-07
Filing date: 1984-10-19
Publication date: 1989-10-03

Abstract

ABSTRACT OF THE DISCLOSURE

N-(2,2,6,6-tetraalkyl-4-piperidinyl)-?-(3,5-di-alkyl-4-hydroxyphenyl)-?',?'' dialkylacetamides and N-alkyl-N'-(3,3,5,5-tetraalkyl-2-keto-1-piperazinyl)-?-(3,5-di-alkyl-4-hydroxyphenyl)?'.?''-dialkylacetamides prepared by a new process are novel stabilizers for or-ganic materials subject to attack and degradation, and form useful combinations for this purpose with other stabilizers against attack of polymer materials by heat, oxygen and light.

Description

N-(SUBSTITUTED CYCLIC ALKYLENEIMINE)-~ --(3,5-DI-ALKYL-4-HYDROXYPHENYL)-~',~''--DIALKYL ACETAMIDES
.

SUMMARY OF THE INVENTION
.

: Novel N-(substituted cyclic alkyleneimi.ne)-~
-(3,5-di-alkyl-4-hydroxyphenyl)-~' ~''-dialkyl acetami-des prepared by a new process are novel stabilizers for organic materials subject to attack and degradation by heat, oxygen and light, and form useful combinations for this purpose with other hindered phenol stabllizers.

DETAILED DESCRIPTION

The novel N-(substituted cyclic alkyleneimi-ne)-d-~3,5-di-alkyl-4-hydroxyphenyl~-~',~''-dialkyl ace-tamides of this invention have the general formula ,OH
~r A
C=O
R5 ~ $

.. I/x~f~y R ~ ~ R9 ~ .

~ ;'f~

wherein Rl and R2 are hydrogen or alkyl and cycloalkyl groups containing 1 to 12 carbon atoms, alkylcycloalkyl and aryl or alkaryl groups wherein the alkyl groups con-tain 1 to 8 carbon atoms, and the aryl groups are nor-mally phenyl or naphthyl; R5, R6, R7, R8 and R9 are hy-drogen, alkyl and cycloalkyl groups containing 1 to 12 carbon atoms, alkylcycloalkyl and aryl or alkaryl groups wherein the alkyl groups contain 1 to 8 carbon atoms, and the aryl groups are normally phenyl or naph-thyl; A is (1) an alkylidene group of the formulaR3-C-R4 wherein R3 and R4 are alkyl groups containing 1 to 18 carbon atoms, Cl-C18, or (2) a cycloalkyl group containing 5 to 12 carbon atoms, and alkaryl groups wherein the alkyl groups contain 1 to 8 carbon atoms, including for example those groups derived from cyclo-hexanone, cycloheptanone, alkyl aryl ketones wherein : ~ the alkyl groups contain 1 to 8 carbon atoms and the : ~ ~ aryl preferably is phenyl or naphthyl, and the like;
`~ B is a bond or an alkylene group oE the formula -(CH2)n-wherein n is 1 to 8, preferably n is 2 to 4; R10 iS
hydrogen or alkyl radicals containing 1 to 18 carbon atoms, O or OH; ~ is N or CH; and Y is H2 or o. Prefer-ably, Rl is an alkyl group containing 1 to 8 carbon atoms, Cl-C8, and R2 is an alkyl group containing 1 to 5 carbon atoms, and more pre~erably at least one of Rl or R2 is a t-alkyl group including t-butyl and t-am-yl; R3 and R4 are alkyl groups containing 1 to 8 carbon atoms, Cl-C8, and more pre~erably 1 to 4 carbon atoms;
R5 is an alkyl group containing 1 to 6 carbon atoms;
R6 and R7 are methyl; R8 is an alkyl group containing 1 to 3 carbon atoms; R~ is an alkyl group containing 1 to ~ carbon atoms; R10 is hydrogen; in B n is 2 to 4; and X is C~.

~J~

These N-(substituted cyclic alkyleneimines)-~-~3,5-di-alkyl-4-hydroxyphenyl)-~', ~''-dialkyl aceta-mides, more speei~lcally the N-(2,2,6,6-tetraalkyl-4-pipereidinyl~ (3,5-di-alkyl-4-hydroxyphenyl)-~',~
di-alkylacetamides and N~alkyl-N'-(3,3,5,5-tetraalkyl-2-keto-l-piperazinealkyl)-~-(3,5-di-alkyl-4-hydroxyphenyl) -~',~''-dialkylacetamides, are prepared by a new process by reacting a 2,6-di-alkylphenol with an aliphatic, cy-cloaliphatic or alkaryl ketone, a haloform and a piper-idine or piperazine compound in the presence of alkalimetal hydroxide. An organic solvent may be used, or large amounts of the ketone reactant may be employed.
The amide is isolated in excellent yields by crystalli-zing the filtered reaction product.
Typical 2,6-dialkyl phenols used have the formula OH
Rl--~R2 wherein Rl and R2 have the meanings set forth above, including 2-methyl-6-t-butylphenol, 2-ethyl-6-t-but-: 20 ylphenol~ 2-propyl-6-t-butylphenol, 2-isopropyl-6-t-butylphenol, 2-n-butyl-6-t-butylphenolt 2,6-di-t-bu-tylphenol, 2-n-amyl-6-t-butylphenoll 2-isoamyl-6-t-butylphenol, 2-hexyl-6-t-butylphenol, 2~heptyl-6-t-butylphenol, 2-isooctyl-6-t-butylphenol, 2-isopropyl-6-methylphenol, 2-n-butyl-6-isopropylphenol, 2-isoamyl--6-ethylphenol, 2-isoamyl-6-methylphenol, 2-isooctyl-6-methylphenol, 2-isooctyl-6-ethylphenol, 2-isooctyl-6-n-propylphenol, 2-isooctyl-6-n-hexylphenol, and the like.
The ketones used include dialkyl ketones, 3~3 Cycloalkanones r alkylcycloalkanones, and alkyl aryl ke-tones. Typical ketones that may be used in the novel process to make the new 3,5-dialkyl-4-hydroxyphenyl-substituted acetic acids of the invention are alkyl ketones of the formula o wherein R3 and R~ are alkyl radicals containing 1 to 18 carbon atoms, preferably 1 to 8 carbon atoms, Cl-C8, including for example acetone, methyl ethyl ke-tone, methyl n-propyl ketone, diethyl ketone, 2-hexa-none, 3,hexanone, di-n-propyl ketone~ 2-octanone, methyl isopropyl ketone, and the like~ Also useful are the cycloalkane ketones containing S to 12 car-bon atoms in the cyclic ring such as cyclobutanone, cyclopentanonel cyclohexanone, cycloheptanone, cyclo-octanone, cyclodecanone, methylcyclopentanone, methyl-cyclohexanone, dicyclohexyl ketone, alkyl aryl ketones when the alkyl group contains 1 to ~ carbon atoms such as acetophenone, o-methoxyacetophenone, p-chloroaceto-phenone, and the like; in amounts from at least about1 mole of ketone per mole o~ 2,6-dialkylphenol, up to amounts sufficient for the ketones to be the solvent of the reaction, 10 moles or more, No more than about two moles is preferred when the ketone is a reactant only. Use of less than 1 mole reduces the product yield, and more than about 2 moles is unnecessary un-less the ketone is the solvent.
The haloform, such as chloroform, is also used in a molar ratio of at least about one mole per mole of 2,6-dialkylphenol used, but preferabl~ a slight molar excess is used up to about a 50 percent molar excess, i.e., 1.5 mole per mole of 2,6-dialkyl-

2.~

phenol. While larger amounts may be used, there isno advantage realized, and lesser amounts will decrease the ultimate yield of the desired product~ Bromoform may be substituted for the chloroform and excellent results will be obtained.
The alkali metal hydroxide is used in pow-der form, or in solution, and includes sodium hydro-xide and potassium hydroxide. Preferablyr a molar excess of the alkali metal hydroxide is used in re-lation to the amount of 2,6-dialkylphenol present.
Normally from about 4 moles of alkali metal hydroxide per mole of 2,6-dialkylphenol up to 10 or more moles may be used, but the amount used preferably is about 4 to about 8 moles of hydroxide per mole of 2,6-di-alkylphenol. Use of less than about 4 moles willreduce the yield of desired product.
The N-substituted cyclic alkyleneimines used in the process of this invention to make the novel acetamides, the piperidines and the piperazines, have the general formula B
~X~Y

R6 ~ ~ R9 wherein R5, R6, R7, R8 and R9 are hydrogen, alkyl, cy-cloalkyl or alkaryl radicals containing 1 to 18 carbon atoms, more preferably wherein the alkyl groups contain 1 to 8 carbon atoms, R10 is hydrogen, alkyl or alkaryl as defined above, oxygen or hydroxyl; X is N or CH; Y

is H2 or O, more preferably X is CH; B is a bond or an alkylene group of the formula -(CH2)n- wherein n is 1 to 8, preferably n is 2 to 4. Typical compounds are substituted piperidine and piperizine derivatives such as 4-amino-Z,2,6,6-tetramethy] piperidine, N'-(2-iso-propylaminoethyl)-3,3,5,5-tetramethyl-2-piperazinone, N'-(2-cyclohexylamino ethyl)-3,3,5,5-tetramethyl-2-pip-erazinone, 4-methylamino-2,2,6,6-tetramethyl piperidi-ne, Nl-(20-isobutylaminoethyl)-3,5,5-trimethyl-3-iso-butyl-2-piperazinone, N,N'-(2,2,6,6-tetramethyl-4-pip-eridyl)-1,6-hexanediamine, and the like.
The amount of substituted piperidine or pipe-razine used in the reaction is based on one mole of the 2,6-dialkylphenol, While the amount may vary from less than a stoichiometric amount, resulting in low product yield, to larger excesses that are not required and have to be separated from the reaction mixture, normal-~ly about 1 to 4 moles to about 1 mole is used~
; The solvent used may be any polar organic solvent, including an excess of the ketone used in place of an added solvent. Typical solvents that may be used include methylene chloridel tetrahydrofuran, diethyl ether, dibutyl ether, dimethyl sulfoxide, 1,4-dioxane, carbon tetrachloride, toluene, xylene, and the like. The amounts of solvent used will vary from about -5 moles to 100 moles per mole of 2,6-dialkylphenol used. As has been stated, the solvent may be elimina-ted if an excess of the reactant ketone is used. In this case, the amount of ketone used, based on the moles of 2,6-dialkylphenol used may be from about 5 to about 20, preferably about 7.5 to 15 moles per mole of 2,6-dialkylphenol.

3~i While the reactants may be added in any order, it is preferred that the alkali metal hydrox-ide be added last, over a period of time to control the exothermic reaction and preferably maintain the S reaction below 30C, preferably below about 10C. The reaction temperature may be varied from about 0C to about 30C, but preferably is conducted from about 0C
to 10C. The reaction time normally will vary from about 5 to about 15 hours.
The amides are readily isolated from the re-action mixture by filtration, washing the filtrate with aqueous inorganic acid, including hydrochloric or sulfuric acid, to the reaction mixture to isolate the amide, most of which is in the organic layer that forms~ The aqueous layer may be extracted with solvent to remove all traces of the amide, and this is added to the other organic layer and this mixture is dried with a desiccant such as anhydrous sodium sulfate, and heat-ed to dryness. This product may be recrystallized if desired.
The practice of the invention is demonstra-ted in the following Examples. The structures of the amides of the following Examples were confirmed by in-frared and nuclear magnetic resonance spectra. Mole-cular weights were determined and confirmed by field desorption mass spectra ~FD/M~). Elemental analysis of carbon and hydrogen was done and the amounts found - were consistent with the Eormulas oE the materials.
.

~XAMPLE 1 N-methyl-N'-(2,2,6,6~tetramethyl-4-piperidinyl)-2-(3,5-di-t-butyl-4-hydroxyphenyl)-2-methyl propionamide 0.1 Mole of 2,6-di-t-butylphenol, 1.0 mole of acetone, 0.15 mole of chloroform and 0.1 mole of 4-methylamino-2,2,6,6~tetramethylpiperidine were added to a reactor and mixed by stirring while being cooled to 5C by a circulating cold bath. 0.5 mole of powdered sodium hydroxide was slowly added in small portions over a period of 1 hour. The reaction mixture was stirred at 10C overnight. The reaction mix from the reactor was filtered. The solid residue was washed with methylene chloride and the wash added to the fil-trate. The filtrate was washed with 50 ml 4N hydro-chloric acid, 50 ml of 5% sodium carbonate, and wasthen dried over sodium sulfate. The filtrate was eva-porated to dryness and the dried product wa~ washed with hexane. The resulting amide was a white solid that had a melting point of 168-173C and a molecular ~; 20 weight of 44~. By elemental analysis it was determined that the amide contained 75.38~ carbon (75O67~ calcula-ted), 10.76% hydrogen (calculated 10.88%) and 6.20 nitrogen (calculated 6.30%).

- N-Isopropyl-N'-[2-(3,3,5,5-tetramethyl-1-piperazinyl)]ethyl-2-(3,5-di-t-butyl-4-hydroxyphenyl)-2~methylpropionamide 0.1 Mole of 2,6-di-t-butylphenol, 1.0 mole 3~, of acetone, 0.15 mole of chloroform, 0.1 mole of N'-(2-isopropylaminoethyl-3,3,5,5-tetramethyl-2-piperizinone were added to a reactor and mixed by stirring while being cooled by a circulating cold bath. 0.5 mole of powdered sodium hydroxide was slowly added over a peri-od of 1 hour. The reaction mixture was stirred at 10C
overnight. The reaction mix from the reactor was fil-tered. The solid residue was washed with methylene chloride and the wash added to the filtrate. The filtrate was washed with 50 ml of 4N hydrochloric acid, 50 ml of 5~ sodium carbonate and was then dried over sodium sulfate. The filtrate was evaporated to dryness and the dried product was washed with hexane. The re-sulting amide was a white solid that had a melting 15 point of 165-169C and a molecular weight of 515. By elemental analysis it was determined that the amide contained 72.~3~ carbon (72.19% calculated), 10.26~ hy-drogen (calculated 10.36~) and 8.02% nitrogen (calcu-lated 8.15%).

N-(2,2,6,6-tetramethyl-~-piperidinyl)-N'-[2-(3,5-di-t-butyl-4-hydroxyphenyl)-2-methyl propanecarboxyl]-1,6-hexanediamine 0,2 mole of 2,6-di-t-butylphenol, 1.0 mole of acetone, 0.15 mole of chloroform, 0.1 mole of 4-hexami-- 25 no-2,2,6,6-tetramethyl piperidine were added to a reac-tor and mixed by stirring while being cooled by a cir-culating cold bath. O.S mole of powdered sodium hydro-xide was slowly added in small portions over a period of 1 hour. The reaction mixture was stirred at 10C

overnight. The reaction mix from the reactor was fil-tered, The solid residue was washed with methylene chloride and the wash added to the filtrate. The fil-trate was washed with 50 ml 4N hydrochloric acid, 50 ml of 5% sodium carbonate and was then dried over so-dium sulfate. The Eiltrate was evaporated to dryness and the dried product was washed with hexane. The resulting amide was a white solid that had a melting point of 255-260C and a molecular weight o~ 983.5.
By elemental analysis it was determined that the amide contained 76.40% carbon (76.38% calculated), 10.71%
hydrogen (calculated 10.90%) and 5.79% nitrogen (cal-culated 5.~4~).

To demonstrate the stabilizing activity of the amides of this invention, test samples of the amides in polypropylene were prepared by mixing the stabilizer compounds with polypropylene in a Brabender Plasticorder fitted with a Cam-Head (mixing chamber)~
The polypropylene is first masticated ~or 1 1~2 minu-~es at 190C. Then the stabili2er is added, followedby 3 minutes additional mixing. The mass is removed and pressed into 20 mil thick sheets. From these sheets are cut 1" x 1" plaques for oven aging. Type C (3`' x 1/8") tensil bars are cut for UV stability tests.
Thermal/oxidative stability (oven aging) tes-- ting consisted of aging the samples in triplicate in an air-circulating oven at 125C. The time to catas-trophic crumbling ~ailure) of the plaque was measured and reported as days to failure. Each sample contained 0.1 weight part of the named amide per 100 weight parts ~6~

of polypropylene (pHr). The following results, in days to failure, were obtained:

Control 2 N-methyl-N'-(2,2,6,6-tetramethyl-4-piperidinyl)-2-(3,5-di-t-butyl-4-hydroxyphenyl)-2-methyl-propionamide 7 N-Isopropyl-N'-[2-(3,3,5,5-tetramethyl-1-piper-azinyl))ethyl-2-(3,5-di-t-butyl-4-hydroxy-phenyl)-2-methylpropionamide 9 Samples containing 0.1 weight part of the a-mide listed below was tested for ultraviolet light sta-bility, i.e., resistance to degradation by UV radiation.
The samples were tested in an Atlas Xenon Weatherometer, Model No. 65-WR, equipped with a 6500 watt Xenon burn-er tube in accordance with ASTM #D2565-79-A. The black panel temperature was 60C. The samples were subjected to an 18~minute water cycle ev~ry 2 hours. The time in hours to a 50% loss in tensile strength was deter-mined. For comparison purposes a samples with no amidewas tested. The following results, in hours, were ob-tained:
Hours Blank (Control) 220 N-Isopropyl-N'-[2-(3,3,5/5-tetramethyl-1-piper-aæin 2-onyl)ethyl]-2-(3,5-di-t-butyl-4-hydroxy-- phenyl)-2-methylpropionamide (0.1 phr) 1280 The N-(2,2,6,6-tetraalkyl-4-piperidinyl)-3,5-di-alkyl-4 hydroxyphenyl)-~',c~ dialkylacetamides and N-alkyl-N'-(3,3,5,5-tetraalkyl-2-keto-1-piperazin-Jl3~:~

ealkyl)_~-(3,5-di-alkyl-4-hydroxyphenyl)~',~''-dialkyl-acetamides as defined herein provide exceptional heat stabiity and resistance to ultraviolet degradaticn to polyolefin polymers. They are especially useful for the stabilization of ~-monoolefin homopolymers and co-polymers, wherein the ~-monoolefin contains 2 to about 8 carbon atoms. High and low-density polyethylene, isotactic and atactic polypropylene, polyisobutylene, and poly(4-methyl-l-pentene) have excellent resistance to heat and oxygen when stabilized with the combina-tions of the present invention. Ethylene-propylene co-polymers and ethylene-propylene terpolymers, generally containing less than about lO percent by weight of one or more monomers containing multiple unsaturatation provided, phenols; ring opened olefin polymers and the like. Polymer blends, that is, physical admixture of two or more polymers may also be stabilized in accord-ance with the present invention.
In addition to polymeric materials, the pre-sent compounds may stabilize a wide variety of other organic materials. Such compounds include: waxes, synthetic and petroleum-derived lubricating oîls and greases; animal oils such as, for example, ~at, tal-low, lard, codliver oil, sperm oil; vegetable oils such as castor, linseed, peanut, palm, cotton seed, and the like; fuel oil, diesel oil, gasoline and the like.
- The (3,5-dialkyl-4-hydroxyphenyl~-substituted amides may be used with other stabilizers including hindered or partially hindered phenols, hindered amine light stabilizers, phosphites, o-hydroxybenzophenones, and the like. Typical hindered phenols are the hydrox-3~

yphenylalkyleneyl isocyanurates such as the symmetrical tris(3,5-di-t-alkyl-4-hydroxybenzyl) isocyanurates; te-trakislmethylene 3-(3',5'-dialkyl-4'-hydroxyphenyl)pro-panoate] methanes wherein the alkyl groups contain 1 to 8 carbon atoms, such as tetrakis[methylene 3-(3',5'-di-t-butyl-4'-hydroxyphenyl)propanoate]methane; alkyl (3-3~,5'-di-t-butyl-4'-hydroxyphenyl)propionates wherein the alkyl groups contain 1 to 18 carbon atoms, such as octadecyl 3~(3',5'-di-t-butyl-4-hydroxyphenyl)propion-ate; 1,3,5-trimethyl-2,4,6-tris[3,5-dialkyl-4-hydroxy-benæyl)benzene; 1,3,5-tris(3,5-di-t-butyl-4-hydroxy-hydrocinnamoylethyl)-s-triazine-2,4,6-(lH,3H,5H)-trione;
2,2'-alkylidene bis (4,6-dialkylphenol)-s wherein the alkyl group contains 1 to 8 carbon atoms, such as 2,2'-methylene bis(4,6-di-t-butylphenol), 2,2'-ethylidene bis(4,6-di-t-butylphenol), and 2,2'-methylene bis(4-methyl-6-t-butylphenol), and the like.
For example, the following combinations pro-vided excellent ageing in polypropylene as shown in the Weatherometer: 0.05 phr of N-isopropyl-N'-[2-(3,3, 5,5-tetramethyl-1-piperazin-2-onyl)ethyl]~2-~3,5-di-t-butyl 4-hydroxyphenyl)-2-methylpropionamide, 0.05 phr o~ 1,1'-(1,2-ethanediyl)bis(3,3,5,5-tetramethyl pipera-zinone, and 0.05 phr of 2,2',2''-tris[3(3,5-di-t-butyl-

4-hydroxyphenyl)propionyloxy]ethyl isocyanurate - more than 2,000 hours; 0~125 phr of N-isopropyl-N'-[2-(3,3,

5,5-te~ramethyl-1-piperazin-2-onyl)ethyl]-2-(3,5-di-t-- butyl-4-hydroxyphenyl)-2-methyl propionamide, 0.05 phr of 2,2',2 "-tris[3(3,5-di-t-butyl-4-hydroxyphenyl)pro-pionyloxy]ethyl isocyanurate, and 0.125 phr of 3,9-bis (octadecyloxy)-2,4,8,10-tetraoxa-3 r 9-diphosphaspiro[S, 5]-undecane - more than 2,000 hours.

The compounds are readily incorporated into materialS to be patented by dis~olving or dispersing them with the materials, in liquids, dispersions, so-luations, and solid forms. If the material is a so-lid, especially a polymeric solid such as rubber or aplastic, the compounds can be admixed using mixers such as Banburys, extruders, two-roll mills, and the like, following conventional techniques. One way to disperse the compounds in plastic materials is to dissolve or suspend the compounds in a solvent or di-luent, mix the mixture with a plastic in powder or solution form, and then ~vaporate the solvent.
Compositions containing the novel combina-tion of compounds can also contain other known com-pounding ingredients such as fillers like carbon black,silicar metal carbonates, talc, and the like; pigments and colorants; curative ingredients like sulfur and peroxides, and vulcanization accelerators; fungicides;
processing aids, reinforcing agents and standard ingre-dients known to the art. Other ingredients ~nown inthe art as ultraviolet light, thermal and/or oxidative stabilizers can also be used.

Claims

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. N-(substituted cyclic alkyleneimine)-?-(3,5-di-alkyl-4-hydroxyphenyl)-?',?''-dialkyl acetami-des having the general formula wherein R1 and R2 are hydrogen or alkyl and cycloalkyl groups containing 1 to 12 carbon atoms, alkylcycloalkyl and aryl or alkaryl groups wherein the alkyl groups con-tain 1 to 8 carbon atoms; R5, R6, R7, R8 and R9 are hy-drogen, alkyl and cycloalkyl groups containing 1 to 12 carbon atoms, alkylcycloalkyl and aryl or alkaryl groups wherein the alkyl groups contain 1 to 8 carbon atoms, A is (1) an alkylidene group of the formula wherein R3 and R4 are alkyl groups containing 1 to 18 carbon atoms, C1-C18, or (2) cycloalkyl groups containing 5 to 12 carbon atoms, and alkaryl groups wherein the alkyl groups contain 1 to 8 carbon atoms; B
is a bond or alkylene group -(CH2)n- wherein n is 1 to 8; R10 is hydrogen or alkyl radicals containing 1 to 18 carbon atoms, O or OH; X is N or CH; and Y is H2 or O.

2. N-(2,2,6,6-tetraalkyl-4-piperidinyl)-?-(3,5-di-alkyl-4-hydroxyphenyl)-?',?''-dialkylacetamides and N-alkyl-N'-(3,3,5,5-tetraalkyl-2-keto-1-piperazin-yl)-?-(3,5~-di-alkyl-4-hydroxyphenyl-?',?''-dialkylace-tamides of Claim 1 wherein R1 contains 1 to 8 carbon atoms; R2 contains 1 to 5 carbon atoms; R3 and R4 con-tain 1 to 8 carbon atoms, the aryl groups are phenyl or naphthyl; (2) is cyclohexyl, methylcyclohexyl, cyclohe-ptyl, or dicyclohexyl, and R1, R2, R5, R6, R7, R8 and R9 are alkyl groups containing l to 8 carbon atoms, and R10 is hydrogen or an alkyl group containing 1 to carbon atoms; in B n is 2 to 4; and X is CH.

3. The acetamides Gf Claim 2 wherein at least one of R1 and R2 is t-butyl or t-amyl and R3 and R4 are alkyl radicals containing 1 to 4 carbon atoms.

4, N-methyl-N'-(2,2,6,6-tetramethyl-4-piper--dinyl)-2-(3,5-di-t-butyl-4-hydroxyphenyl)-2-methylpro-pionamide of Claim 3.

5. N-isopropyl-N'-[2-(3,3,5,5-tetramethyl-1-piperazin-2-onyl)ethyl]-2-(3,5-di-t-butyl-4-hydroxyphe-nyl)-2-methylpropionamide of Claim 3.

6. N-(2,2,6,6-tetramethyl-4-piperidinyl)-N'-[2-(3,5-di-t-butyl-4-hydroxyphenyl)-2-methylpropanecar-boxy-1]-1,6-hexanediamine of Claim 3.

7. A composition comprising (1) organic ma-terials subject to degradation and stabilizing amounts of (2) N-(substituted cyclic alkyleneimine)-?-(3,5-di-alkyl-4-hydroxyphenyl)-?',?''-dialkyl acetamides hav-ing the general formula wherein R1 and R2 are hydrogen or alkyl and cycloalkyl groups containing 1 to 12 carbon atoms, alkylcycloalkyl and aryl or alkaryl groups wherein the alkyl groups con-tain 1 to 8 carbon atoms; R5, R6, R7, R8 and R9 are hy-drogen, alkyl and cycloalkyl groups containing 1 to 12 carbon atoms, alkylcycloalkyl and aryl or alkaryl groups wherein the alkyl groups contain 1 to 8 carbon atoms; A is (1) an alkyidene group of the formula wherein R3 and R4 are alkyl groups containing 1 to 18 carbon atoms, C1-C18, or (2) a cycloalkyl group containing 5 to 12 carbon atoms, and alkaryl groups wherein the alkyl groups contain 1 to 8 carbon atoms;
R10 is hydrogen or alkyl radicals containing 1 to 18 carbon atoms, O or OH; X is.N or CH; Y is H2 or O; and B is a bond or alkylene group -(CH2)n- wherein n is 1 to 8.
8 Compositions of Claim 7 wherein R1 con-tains 1 to 8 carbon atoms; R2 contains 1 to 5 carbon atoms; R3 and R4 contain 1 to 8 carbon atoms; (2) is cyclohexyl, methylcyclohexyl, cycloheptyl, or dicyclo-hexyl, the aryl groups are phenyl or naphthyl; and R1, R2, R5, R6, R7 and R8 are alkyl groups containing 1 to

8 carbon atoms; and R10 is hydrogen or an alkyl group containing 1 to 8 carbon atoms; in B n is 2 to 4; and X is CH.

9. Compositions of Claim 8 wherein at least one of R1 and R2 is t-butyl or t-amyl and R3 and R4 are alkyl radicals containing 1 to 4 carbon atoms.

10, Compositions of Claim 9 wherein in (1) said organic material is a polymer and (2) is N-methyl-N'-(2,2,6,6-tetramethyl-4-piperidinyl)-2-(3,5-di-t-but-yl-4-hydroxyphenyl)-2-methylpropionamide.

11. Compositions of Claim 9 wherein in (1) said organic material is a polymer and (2) is N-isopro-pyl-N'-[2-(3,3,5,5-tetramethyl-1-piperazin-2-onyl)eth-yl]-2-(3,5-di-t-butyl-4-hydroxyphenyl)-2-methylpropion-amide.

12. Compositions of Claim 9 wherein in (1) said organic material is a polymer and (2) is N-(2,2,6, 6-tetramethyl-4-piperidinyl)-N-2-[(3,5-di-t-butyl-4-hy-droxyphenyl)-2-methylpropanecarboxyl]-1,6-hexanediamine.

13. A process for preparing N-(substituted cyclic alkyleneimine)-?-(3,5-di-alkyl-4-hydroxyphen-yl)?,?'-dialkyl acetamides having the general for-mula wherein R1 and R2 are hydrogen or alkyl and cycloalkyl groups containing 1 to 12 carbon atoms, alkylcycloalkyl and aryl or alkaryl groups wherein the alkyl groups con-tain 1 to 8 carbon atoms; R5, R6, R7, R8 and R9 are hy-drogen, alkyl and cycloalkyl groups containing 1 to 12 carbon atoms, alkylcycloalkyl and aryl or alkaryl groups wherein the alkyl groups containing 1 to 8 car-bon atoms; A is (1) an alkyidene group of the formula wherein R3 and R4 are alkyl groups containing 1 to 18 carbon atoms, C1-C18, or (2) a cycloalkyl group containing 5 to 12 carbon atoms, and alkaryl groups wherein the alkyl groups contain 1 to 8 carbon atoms;
R10 is hydrogen or alkyl radicals containing 1 to 18 carbon atoms, O or OH; X is N or CH, B is a bond or al-kylene group -(CH2)n- wherein n is 1 to 8; and Y is H2 or O; comprising reacting together a 2,6-dialkylphenol having the formula wherein R1 and R2 have the meanings above, a ketone se-lected from the group consisting of dialkyl ketones, cycloalakanones, alkcycloalkanones, and alkaryl ketones wherein the alkyl groups contain 1 to 18 carbon atoms, a haloform selected from the group consisting of chloro-form and bromoform, and an alkali metal hydroxide and piperidines and the piperazines, having the general formula wherein R5, R6, R7, R8 and R9 are hydrogen, alkyl, cy-cloalkyl or alkaryl radicals containing 1 to 12 carbon atoms; R10 is hydrogen, alkyl or alkaryl as defined herein, oxygen radical or hydroxyl; X is N or CH; in B
n is 2 to 4; and Y is H2 or O.

14. A process of Claim 13 wherein R1 con-tains 1 to 8 carbon atoms and R2 contains 1 to 5 carbon atoms, the ketone is a dialkyl ketone of the formula wherein R3 and R4 are alkyl radicals containing 1 to 8 carbon atoms, cyclopentanone, cyclohexanone, cyclohep-tanone and alkyl derivatives thereof wherein the alkyl groups contain 1 to 4 carbon atoms, R1, R2, R3, R4, R5, R6, R7, R8 and R9 are alkyl groups containing 1 to 8 carbon atoms, and X is CH.