Piperidine derivatives, their production and use as stabilizers

Claim 2

A piperidine compound by the formula (I), ##STR18## wherein R 1 is a uni- or divalent carboxylic acid residue, R 2 is a hydrogen atom or a C 1 -C 3 alkyl or C 1 -C 18 alkyl carbonyl group, l is an integer of 1 to 3 and n is 1 or 2, said univalent carboxylic acid residue being selected from the group consisting of (a) univalent carboxylic acid residues wherein the carboxylic acid residue is a C 1 -C 20 alkyl group, (b) univalent carboxylic acid residues having a cyclohexyl group linked to the end of the carboxylic acid residue of (a), and (c) univalent carboxylic acid residues having a phenyl group linked to the end of the carboxylic acid residue of (a), said divalent carboxylic acid residue being selected from the group consisting of (d) divalent carboxylic acid residues wherein the carboxylic acid residue is a C 1 -C 18 alkyl group, (e) divalent carboxylic acid residues wherein the carboxylic acid residue is a single bond, (f) divalent carboxylic acid residues wherein the carboxylic acid residue is a C 5 -C- 16 cycloalkyl group, (g) divalent carboxylic acid residues wherein the carboxylic acid residue is an aromatic group having 6 or 10 carbon atoms, (h) divalent carboxylic acid residues wherein the carboxylic acid residue is an alkyl group having a phenyl group linked to the side or main chain, the alkyl moiety having 1 to 16 carbon atoms and (i) C 4 -C 20 divalent carboxylic acid residues having a carbon or sulfur atom in the carboxylic acid residue.

Claim 3

A method for producing a piperidine compound represented by the formula (I), ##STR19## wherein R 1 is a uni- or divalent carboxylic acid residue, R 2 is a hydrogen atom or a C 1 -C 3 alkyl or C 1 -C 18 alkyl carbonyl group, l is an integer of 1 to 3 and n is 1 or 2, characterized in that an iminodialkanoic acid compound represented by the formula (II), ##STR20## wherein R 1 , l and n have the same meanings as described in claim 1, and R 3 is a C 1 -C 4 alkyl group, is reacted with a piperidinol compound represented by the formula (III), ##STR21## wherein R 2 has the same meaning as described in claim 1.

Claim 4

A method as claimed in claim 2 wherein the reaction is carried out in the presence of a solvent selected from the group consisting of aromatic hydrocarbons, aliphatic hydrocarbons, alicyclic hydrocarbons, water-soluble polar solvents, ethers and alcohols.

Claim 5

A method as claimed in claim 2 wherein the reaction is carried out in the presence of a basic catalyst.

Claim 6

A method as claimed in claim 4 wherein the basic catalyst is selected from the group consisting of metal hydroxides, metal hydrides, metal amides, alkali metal alkoxides and alkali metal phenoxides.

Claim 7

A method as claimed in claim 2 wherein the reaction is carried out at a temperature in the range of 0° to 200° C.

Claim 8

A method as claimed in claim 2 wherein the molar ratio of the piperidinol compound of the formula (III) to the iminodialkanoic acid derivative of the formula (II) is in the range of 2:1 to 5:1 when n is 1, and 4:1 to 10:1 when n is 2.

Claim 9

A method for producing a piperidine compound represented by the formula (I) ##STR22## wherein R 1 is a uni- or divalent carboxylic acid residue, R 2 is a hydrogen atom or a C 1 -C 3 alkyl or C 1 -C 18 alkyl carbonyl group, l is an integer of 1 to 3 and n is 1 or 2, characterized in that an iminodialkanoic acid compound represented by the formula (IV), ##STR23## wherein R 2 and l have the same meanings as described in claim 1, is reacted with a carboxylic acid halide represented by the formula (V), ##STR24## wherein R 1 and n have the same meanings as described in claim 1, and X is a halogen atom.

Claim 10

A method as claimed in claim 8 wherein the reaction is carried out in an inert solvent in the presence of a dehydrohalogenating agent.

Claim 11

A method as claimed in claim 9 wherein the inert solvent is selected from the group consisting of aliphatic hydrocarbons, alicyclic hydrocarbons, aromatic hydrocarbons, water-soluble polar solvents, ethers, halogenated hydrocarbons and esters.

Claim 12

A method as claimed in claim 8 wherein the molar ratio of the iminodialkanoic acid compound of the formula (IV) to the uni- or divalent carboxylic acid halide of the formula (V) is in the range of 0.9:1 to 1.1:1 for the univalent carboxylic acid halide and 1.8:1 to 2.2:1 for the divalent carboxylic acid halide.

Claim 13

A method as claimed in claim 8 wherein the reaction is conducted at a temperature in the range of -30° to 120° C.

Claim 14

A stabilizer for organic substances containing a piperidine compound represented by the formula (I), ##STR25## wherein R 1 is a uni- or divalent carboxylic acid residue, R 2 is a hydrogen atom or a C 1 -C 3 alkyl or C 1 -C 18 alkyl carbonyl group, l is an integer of 1 to 3 and n is 1 or 2, as an effective ingredient, said univalent carboxylic acid residue being selected from the group consisting of (a) univalent carboxylic acid residues wherein the carboxylic acid residue is a C 1 -C 20 alkyl group, (b) univalent carboxylic acid residues having a cyclohexyl group linked to the end of the carboxylic acid residue of (a), and (c) univalent carboxylic acid residues having a phenyl group linked to the end of the carboxylic acid residue of (a), said divalent carboxylic acid residue being selected from the group consisting of (d) divalent carboxylic acid residues wherein the carboxylic acid residue is a C 1 -C 18 alkyl group, (e) divalent carboxylic acid residues wherein the carboxylic acid residue is a single bond, (f) divalent carboxylic acid residues wherein the carboxylic acid residue is a C 5 -C-.sub. 16 cycloalkyl group, (g) divalent carboxylic acid residues wherein the carboxylic acid residue is an aromatic group having 6 or 10 carbon atoms, (h) divalent carboxylic acid residues wherein the carboxylic acid residue is an alkyl group having a phenyl group linked to the side or main chain, the alkyl moiety having 1 to 16 carbon atoms and (i) C 4 -C 20 divalent carboxylic acid residues having a carbon or sulfur atom in the carboxylic acid residue.

Claim 15

A stabilizer for organic substances containing a piperidine compound represented by the formula (I), ##STR25## wherein R 1 is a uni- or divalent carboxylic acid residue, R 2 is a hydrogen atom or a C 1 -C 3 alkyl or C 1 -C 18 alkyl carbonyl group, l is an integer of 1 to 3 and n is 1 or 2, as an effective ingredient, said univalent carboxylic acid residue being selected from the group consisting of (a) univalent carboxylic acid residues wherein the carboxylic acid residue is a C 1 -C 20 alkyl group, (b) univalent carboxylic acid residues having a cyclohexyl group linked to the end of the carboxylic acid residue of (a), and (c) univalent carboxylic acid residues having a phenyl group linked to the end of the carboxylic acid residue of (a), said divalent carboxylic acid residue being selected from the group consisting of (d) divalent carboxylic acid residues wherein the carboxylic acid residue is a C 1 -C 18 alkyl group, (e) divalent carboxylic acid residues wherein the carboxylic acid residue is a single bond, (f) divalent carboxylic acid residues wherein the carboxylic acid residue is a C 5 -C-.sub. 16 cycloalkyl group, (g) divalent carboxylic acid residues wherein the carboxylic acid residue is an aromatic group having 6 or 10 carbon atoms, (h) divalent carboxylic acid residues wherein the carboxylic acid residue is an alkyl group having a phenyl group linked to the side or main chain, the alkyl moiety having 1 to 16 carbon atoms and (i) C 4 -C 20 divalent carboxylic acid residues having a carbon or sulfur atom in the carboxylic acid residue.

Claim 16

A stabilizer as claimed in claim 13 which further contains a phosphite type antioxidant.

Claim 17

A stabilizer as claimed in claim 14 wherein the phosphite type antioxidant is selected from the group consisting of tris(nonylphenyl)phosphite, distearyl pentaerythritol diphosphite, tris(2,4-di-tert-butylphenyl)phosphite, tris(2-tert-butyl-4-methylphenyl)phosphite, bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphite and tetrakis(2,4-di-tert-butylphenyl)4,4'-biphenylene diphosphite.

Claim 18

A stabilizer as claimed in claim 13 which further contains a sulfur-containing antioxidant.

Claim 19

A stabilizer as claimed in claim 16 wherein the sulfur-containing antioxidant is selected from the group consisting of dilauryl thiodipropionate, dimyristyl thiodipropionate, distearyl thiodipropionate, pentaerythritol tetrakis(β-laurylthiopropionate) and pentaerythritol tetrakis(β-hexylthiopropionate).

Claim 20

A stabilized organic material stabilized by the stabilizer according to any of claims 13.

Claim 21

A stabilized organic material stabilized by the stabilizer according to any of claims 14 to 17.

Claim 22

A stabilized organic material as claimed in claim 18 or 19 wherein the organic material stabilized is a synthetic resin selected from low-density polyethylene, high-density polyethylene, linear low-density polyethylene, chlorinated polyethylene, EVA resin, polypropylene, polyvinyl chloride, methacrylic resin, polystyrene, impact-resistant polystyrene, ABS resin, AES resin, MBS resin, polyethylene terephthalate, polybutylene terephthalate, polyamide, polyimide, polycarbonate, polyacetal, polyurethane, and unsaturated polyester resin.

Claim 23

A stabilized organic material as claimed in claim 18 or 19 wherein the organic material stabilized is selected from oil paints, spirit paints, cellulose derivative paints, synthetic resin paints, synthetic resin emulsion paints and water-based baking paints.

Claim 24

A stabilized organic material as claimed in claim 18 wherein the amount of the stabilizer is 0.01 to 5 parts by weight based on 100 parts by weight of the organic material.