Preparation of cyanate esters

Claim 2

A process for preparing a cyanate ester comprising the steps of: (a) contacting, at a temperature within the range of about 40° to about 80° C., (i) a phenolic compound which can be represented by the formula ##STR3## in which each a and b is independently 0, 1, 2 or 3 and at least one a is not 0; n is within the range of 0 to about 8; each R is selected independently from hydrogen, C 1-6 alkyl, C 1-6 allyl, halide, C 1-6 alkoxy, maleimide, propargyl ether, glycidyl ether, and phenyl; and A is a divalent linking moiety, and (ii) a tertiary amine which can be represented by the formula ##STR4## in which R', R" and R'" are independently selected from C 1-10 alkyl, phenyl and C 1-7 cycloalkyl, under conditions effective for production of a reaction product of said phenolic compound and said tertiary amine; and subsequently (b) contacting, at a temperature within the range of about 20° to 60° C., said reaction product and a cyanogen halide under conditions effective for preparation of a cyanate ester.

Claim 3

The process of claim 1 in which the tertiary amine is selected from the group consisting of trimethyl amine, triethyl amine, methyl diethyl amine, tripropyl amine, tributyl amine, methyl dibutyl amine, dinonyl methyl amine, dimethyl stearyl amine, dimethyl cyclohexyl amine and diethyl aniline.

Claim 4

The process of claim 1 in which the cyanogen halide is selected from the group consisting of cyanogen chloride and cyanogen bromide.

Claim 5

The process of claim 3 in which the tertiary amine is triethyl amine.

Claim 6

The process of claim 1 in which the phenolic compound is selected from the group consisting of phenol, dihydroxy benzene and 2,2-bis(p-hydroxyphenyl)propane.

Claim 7

The process of claim 1 in which the phenol can be described by the formula ##STR5## in which A is C 1-3 alkyl, each R is selected from hydrogen, halide and C 1-3 alkylene and b is 0, 1, 2 or 3.

Claim 8

The process of claim 1 in which the phenolic compound is a phenolic novolac.

Claim 9

The process of claim 1 in which the base is triethylamine.

Claim 10

The process of claim 8 in which step (b) is carried out in methyl isobutyl ketone solvent.

Claim 11

The process of claim 1 which further comprises the step of recovering a solid cyanate ester.

Claim 12

A process for preparing an aromatic cyanate ester having propargyl ether substituents, the process comprising: (a) contacting (i) a phenolic compound which can be represented by the formula ##STR6## in which each a and b is independently 0, 1, 2 or 3 and at least one a is not 0; n is within the range of 0 to about 8; each R is selected independently from hydrogen, C 1-6 alkyl, C 1-6 allyl, halide, C 1-6 alkoxy, maleimide, propargyl ether, glycidyl ether, and phenyl and at least one R is propargyl ether; and A is a divalent linking moiety, and (ii) less than an equivalent amount, based on phenolic hydroxyl groups, of a propargyl halide in a basic reaction medium under conditions effective to produce a phenolic product having propargyl ether substituents; (b) reacting, at a temperature within the range of about 40° to about 80° C., said phenolic product with at least about 0.7 equivalent, based on remaining phenolic hydroxyl groups, of a tertiary amine which can be represented by the formula ##STR7## in which R', R" and R'" are selected independently from C 1-10 alkyl, phenyl and C 1-7 cycloalkyl, under conditions effective for production of a reaction product of said phenolic compound and said tertiary amine; and subsequently (c) contacting said reaction production and a cyanogen halide in a liquid reaction medium at a temperature within the range of about 20° to about 60° C. to produce said aromatic cyanate ester having propargyl ether substitutents.

Claim 13

A process for preparing an aromatic cyanate ester having propargyl ether substituents, the process comprising: (a) contacting (i) a phenolic compound which can be represented by the formula ##STR6## in which each a and b is independently 0, 1, 2 or 3 and at least one a is not 0; n is within the range of 0 to about 8; each R is selected independently from hydrogen, C 1-6 alkyl, C 1-6 allyl, halide, C 1-6 alkoxy, maleimide, propargyl ether, glycidyl ether, and phenyl and at least one R is propargyl ether; and A is a divalent linking moiety, and (ii) less than an equivalent amount, based on phenolic hydroxyl groups, of a propargyl halide in a basic reaction medium under conditions effective to produce a phenolic product having propargyl ether substituents; (b) reacting, at a temperature within the range of about 40° to about 80° C., said phenolic product with at least about 0.7 equivalent, based on remaining phenolic hydroxyl groups, of a tertiary amine which can be represented by the formula ##STR7## in which R', R" and R'" are selected independently from C 1-10 alkyl, phenyl and C 1-7 cycloalkyl, under conditions effective for production of a reaction product of said phenolic compound and said tertiary amine; and subsequently (c) contacting said reaction production and a cyanogen halide in a liquid reaction medium at a temperature within the range of about 20° to about 60° C. to produce said aromatic cyanate ester having propargyl ether substitutents.

Claim 14

The process of claim 11 in which the tertiary amine is triethylamine.

Claim 15

The process of claim 11 in which the phenolic compound is selected from 2,2-bis(p-hydroxyphenyl)propane and phenolic novolacs.

Claim 16

The process of claim 11 in which the tertiary amine of step (b) comprises triethylamine.