Process for squaraine compositions from half esters of squaric acid

Claim 2

An improved process for the preparation of squaraine compositions which comprises reacting an alkyl squarate, with an aniline, in the presence of an aliphatic alcohol and an optional acid catalyst.

Claim 3

A process in accordance with claim 1 wherein the reaction is accomplished at a temperature of from about 60 degrees Centigrade to about 160 degrees Centigrade.

Claim 4

A process in accordance with claim 1 wherein there is further included in the reaction an acid catalyst.

Claim 5

A process in accordance with claim 1 wherein the alkyl squarate is selected from the group consisting of a methyl squarate, ethyl squarate, propyl squarate, butyl squarate, pentyl squarate, hexyl squarate or heptyl squarate.

Claim 6

A process in accordance with claim 1 wherein the aniline is selected from the group consisting of a N,N-dimethyaniline, N,N-diethylaniline, N,N-dipropylaniline, N,N-dibutylaniline, N,N-dipentylaniline, 3-fluoro-N,N-dimethylaniline, 3-hydroxy-N,N-dimethylaniline, 3-methyl-N,N-dimethylaniline, and 3-hydroxy-N,N-diethylaniline.

Claim 7

A process in accordance with claim 1 wherein the aliphatic alcohol is 1-butanol, 1-propanol, or amyl alcohol.

Claim 8

A process in accordance with claim 1 wherein the resulting squaraine product is bis(2-fluoro-4-dimethylaminophenyl)squaraine.

Claim 9

A process in accordance with claim 1 wherein the resulting squaraine product is bis(4-dimethylaminophenyl)squaraine.

Claim 10

A process in accordance with claim 1 wherein the resulting squaraine product is bis(2-hydroxy-4-dimethylaminophenyl)squaraine.

Claim 11

A process in accordance with claim 1 wherein the resulting squaraine product is bis(2-methyl-4-dimethylaminophenyl)squaraine, or bis(2-hydroxy-4-diethylaminophenyl)squaraine.

Claim 12

A process in accordance with claim 1 wherein the alkyl squarate is methyl squarate.

Claim 13

A process in accordance with claim 2 wherein there is selected from about 5 millimoles to about 50 millimoles of the alkyl squarate, from about 0.05 milliliter to about 1 milliliter of sulfuric acid, from about 10 millimoles to about 100 millimoles of aniline, and from about 5 milliliters to about 200 milliliters of aliphatic alcohol.

Claim 14

A process in accordance with claim 2 wherein the reaction temperature is from about 98 degrees Centigrade to about 140 degrees Centigrade.

Claim 15

A process in accordance with claim 2 wherein the acid catalyst is sulfuric acid, trichloroacetic acid, or oxalic acid.

Claim 16

A process for the preparation of squaraine compositions which comprises reacting in the presence of an optional acid catalyst and an aliphatic alcohol an alkyl squarate of the following formula with an aniline of the following formula: ##STR3## wherein R, R 1 , R 2 , are independently selected from alkyl groups, and R 3 is an alkyl group, a hydroxy group, hydrogen, or fluorine, Ar is an aromatic group, and n is the number zero or one.

Claim 17

A process for the preparation of squaraine compositions which comprises reacting in the presence of an optional acid catalyst and an aliphatic alcohol an alkyl squarate of the following formula with an aniline of the following formula: ##STR3## wherein R, R 1 , R 2 , are independently selected from alkyl groups, and R 3 is an alkyl group, a hydroxy group, hydrogen, or fluorine, Ar is an aromatic group, and n is the number zero or one.

Claim 18

A process in accordance with claim 15, wherein R, R 1 , R 2 , and R 3 , are alkyl groups containing from about one carbon atom to about ten carbon atoms.

Claim 19

A process in accordance with claim 15, wherein R is methyl, Ar is phenyl, R 1 is methyl, R 2 is methyl, and n is zero.

Claim 20

A process in accordance with claim 15, wherein the reaction is accomplished at a temperature of from about 60 degrees Centigrade to about 160 degrees Centigrade.