Process for the production of 2-aryl-2H-benzotriazoles

Claim 2

A process for the production of 2-aryl-2H-benzotriazoles of the formula I ##STR27## wherein R 1 is hydrogen or chlorine, R 2 is hydrogen, chlorine, lower alkyl of 1 to 4 carbon atoms, lower alkoxy of 1 to 4 carbon atoms, carboalkoxy of 2 to 9 carbon atoms, carboxy or --SO 3 H, R 3 is alkyl of 1 to 12 carbon atoms, alkoxy of 1 to 4 carbon atoms, phenyl, phenyl substituted with alkyl groups, said alkyl groups having 1 to 8 carbon atoms, cycloalkyl of 5 to 6 carbon atoms, carboalkoxy of 2 to 9 carbon atoms, chlorine, carboxyethyl or phenylalkyl of 7 to 9 carbon atoms, R 4 is hydrogen, lower alkyl of 1 to 4 carbon atoms, lower alkoxy of 1 to 4 carbon atoms, chlorine or hydroxyl, and R 5 is hydrogen, alkyl of 1 to 12 carbon atoms, chlorine, cycloalkyl of 5 to 6 carbon atoms or phenylalkyl of 7 to 9 carbon atoms, which comprises reducing and cyclizing the corresponding o-nitro-azobenzene ##STR28## with hydrogen at a temperature in the range of from about 20° C. to about 100° C. and at a pressure in the range from about 15 psia (1.05 kg/cm 2 , 1 atmosphere) to about 1000 psia (70 kg/cm 2 , 66 atmospheres) while mixed in an alkaline medium, said medium consisting essentially of an organic solvent containing a water-soluble amine and having a pH greater than 10 in the presence of a nickel hydrogenation catalyst, separating the catalyst which is suitable for recycle, and recovering the desired 2-aryl-2H-benzotriazole.

Claim 3

A process according to claim 1 wherein said catalyst is a promoted nickel hydrogenation catalyst.

Claim 4

A process according to claim 2 wherein said hydrogenation catalyst is molybdenum-promoted Raney nickel or chromium-promoted Raney nickel.

Claim 5

A process according to claim 3 wherein said hydrogenation catalyst is molybdenum-promoted Raney nickel.

Claim 6

A process according to claim 1 which further comprises, carrying out the reduction and cyclization in an solvent system containing an organic amine, removing the nickel catalyst by filtration, and recovering the desired 2-aryl-2H-benzotriazole.

Claim 7

A process according to claim 1 which further comprises, carrying out the reduction and cyclization in an organic solvent system consisting essentially of an aliphatic or alicyclic amine or morpholine, removing the nickel catalyst by filtration, and recovering the desired 2-aryl-2H-benzotriazole.

Claim 8

A process according to claim 1 wherein said alkaline medium is a solution of a aromatic hydrocarbon, methanol and an aliphatic or alicyclic amine or morpholine.

Claim 9

A process according to claim 1 wherein said alkaline medium is a solution of an alkanol and an aliphatic or alicyclic amine or morpholine.

Claim 10

A process according to claim 1 wherein said alkaline medium is an aliphatic or alicyclic amine or morpholine.

Claim 11

A process according to claim 1 for the production of a compound of formula I wherein R 1 is hydrogen, R 2 is hydrogen, chlorine, lower alkyl of 1 to 2 carbon atoms, methoxy or carboxy, R 3 is alkyl of 1 to 12 carbon atoms, cyclohexyl, phenyl, chlorine, α-methylbenzyl or carboxyethyl, R 4 is hydrogen, hydroxyl or methyl, and R 5 is hydrogen, alkyl of 1 to 12 carbon atoms, chlorine, cyclohexyl, benzyl or α-methylbenzyl.

Claim 12

A process according to claim 1 for production of a compound of formula I wherein R 1 is hydrogen, R 2 is hydrogen or chlorine, R 3 is methyl, sec-butyl, tert-butyl, tert-amyl, tert-octyl, cyclohexyl, chlorine or carboxyethyl, R 4 is hydrogen, and R 5 is hydrogen, chlorine, methyl, tert-butyl, sec-butyl, tert-amyl, tert-octyl or α-methylbenzyl.

Claim 13

A process according to claim 1 for the production of 2-(2-hydroxy-5-methylphenyl)-2H-benzotriazole.

Claim 14

A process according to claim 1 for the production of 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole.

Claim 15

A process according to claim 1 for the production of 2-(2-hydroxy-3,5-di-tert-amylphenyl)-2H-benzotriazole.

Claim 16

A process according to claim 1 for the production of 5-chloro-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole.

Claim 17

A process according to claim 1 for the production of 5-chloro-2-(2-hydroxy-3-tert-butyl-5-methylphenyl)-2H-benzotriazole.

Claim 18

A process according to claim 1 for the production of 2-(2-hydroxy-3,5-di-tert butylphenyl)-2H-benzotriazole.

Claim 19

A process according to claim 1 wherein the amine is selected from the group consisting of primary aliphatic amines with alkyl groups of 1 to 6 carbon atoms, secondary aliphatic amines with alkyl groups of 1 to 6 carbon atoms, tertiary aliphatic amines with alkyl groups of 1 to 6 carbon atoms, piperidine, piperazine, morpholine, pyrrolidine and guanidine.

Claim 20

An improved process for the production of 2-aryl-2H-benzotriazoles of the formula I ##STR29## wherein R 1 is hydrogen or chlorine, R 2 is hydrogen, chlorine, lower alkyl of 1 to 4 carbon atoms, lower alkoxy of 1 to 4 carbon atoms, carboalkoxy of 2 to 9 carbon atoms, carboxy or --SO 3 H, R 3 is alkyl of 1 to 12 carbon atoms, alkoxy of 1 to 4 carbon atoms, phenyl, phenyl substituted with alkyl groups, said alkyl groups having 1 to 8 carbon atoms, cycloalkyl of 5 to 6 carbon atoms, carboalkoxy of 2 to 9 carbon atoms, chlorine, carboxyethyl or phenylalkyl of 7 to 9 carbon atoms, R 4 is hydrogen, lower alkyl of 1 to 4 carbon atoms, lower alkoxy of 1 to 4 carbon atoms, chlorine or hydroxyl, and R 5 is hydrogen, alkyl of 1 to 12 carbon atoms, chlorine, cycloalkyl of 5 to 6 carbon atoms or phenylalkyl of 7 to 9 carbon atoms, by reducing and cyclizing the corresponding o-nitroazobenzene ##STR30## with hydrogen at a temperature in the range of from 20° C. to about 100° C. and at a pressure in the range from about 15 psia (1.05 kg.cm 2 1 atmosphere) to about 1000 psia (70 kg/cm 2 , 66 atmospheres) while mixed in an alkaline medium having a pH greater than 10 in the presence of a nickel hydrogenation catalyst and recovering the desired 2-aryl-2H-benzotriazole wherein the improvement comprises using as the alkaline medium an aqueous alkaline or an aqueous hydrocarbon alkaline medium, said medium containing an alkali metal hydroxide and containing from 0.1 to 5% by weight of a dispersing agent which is a polyhydroxyalkyl monoester of a fatty acid.

Claim 21

An improved process for the production of 2-aryl-2H-benzotriazoles of the formula I ##STR29## wherein R 1 is hydrogen or chlorine, R 2 is hydrogen, chlorine, lower alkyl of 1 to 4 carbon atoms, lower alkoxy of 1 to 4 carbon atoms, carboalkoxy of 2 to 9 carbon atoms, carboxy or --SO 3 H, R 3 is alkyl of 1 to 12 carbon atoms, alkoxy of 1 to 4 carbon atoms, phenyl, phenyl substituted with alkyl groups, said alkyl groups having 1 to 8 carbon atoms, cycloalkyl of 5 to 6 carbon atoms, carboalkoxy of 2 to 9 carbon atoms, chlorine, carboxyethyl or phenylalkyl of 7 to 9 carbon atoms, R 4 is hydrogen, lower alkyl of 1 to 4 carbon atoms, lower alkoxy of 1 to 4 carbon atoms, chlorine or hydroxyl, and R 5 is hydrogen, alkyl of 1 to 12 carbon atoms, chlorine, cycloalkyl of 5 to 6 carbon atoms or phenylalkyl of 7 to 9 carbon atoms, by reducing and cyclizing the corresponding o-nitroazobenzene ##STR30## with hydrogen at a temperature in the range of from 20° C. to about 100° C. and at a pressure in the range from about 15 psia (1.05 kg.cm 2 1 atmosphere) to about 1000 psia (70 kg/cm 2 , 66 atmospheres) while mixed in an alkaline medium having a pH greater than 10 in the presence of a nickel hydrogenation catalyst and recovering the desired 2-aryl-2H-benzotriazole wherein the improvement comprises using as the alkaline medium an aqueous alkaline or an aqueous hydrocarbon alkaline medium, said medium containing an alkali metal hydroxide and containing from 0.1 to 5% by weight of a dispersing agent which is a polyhydroxyalkyl monoester of a fatty acid.

Claim 22

An improved process according to claim 19 for the preparation of 2-(2-hydroxy-5-methylphenyl)-2H-benzotriazole.

Claim 23

An improved process according to claim 19 for the preparation of 2-(2-hydroxy-3,5-di-tert-amylphenyl)-2H-benzotriazole.

Claim 24

A process according to claim 19 wherein the dispersing agent is sorbitan monooleate.

Claim 25

A process according to claim 19 wherein said alkaline medium is an aqueous alkali metal hydroxide solution containing a water immiscible hydrocarbon and a dispersing agent.