Process for the preparation of oxalate esters

Claim 2

A process for the preparation of oxalate esters of an alcohol having from 1 to 20 carbon atoms which comprises reacting under substantially anhydrous conditions, a saturated monohydric aliphatic or alicyclic alcohol which may contain other substituents which do not interfere with the reaction or an aromatic alcohol selected from the group consisting of benzyl, chlorobenzyl and methoxy-benzyl alcohols with carbon monoxide at a pressure of between about 1 and 700 atmospheres and at a temperature in the range of about 50° to 250° C. in the presence of an effective amount of a catalyst selected from the group consisting of palladium (II), rhodium (III), platinum (II) and copper (I) or (II) salt compounds and at least a stoichiometric amount of an aliphatic, cycloaliphatic, aromatic or heterocyclic amine or ammonia and at least a stoichiometric amount of a copper (II) or iron (III) oxalate, sulfate, acetate, or trifluroacetate oxidant salt compound and recovering the desired oxalate ester.

Claim 3

A process according to claim 1 wherein the oxidant salt compound is selected from the group consisting of copper (II) sulfate, copper (II) acetate, copper (II) oxalate, copper (II) trifluoroacetate, and iron (III) sulfate.

Claim 4

A process according to claim 2 wherein the oxidant salt compound is copper (II) sulfate.

Claim 5

A process according to claim 1 wherein the reaction is carried out in the present of a co-catalytic amount of an organic mono- or poly-dentate ligand selected from the group consisting of alkyl, aryl and halogen substituted phosphines, arsines and stibines.

Claim 6

A process according to claim 4 wherein the ligand is selected from the group consisting of triethylphosphine, triphenylphosphine, triphenylarsine and triphenylstibine.

Claim 7

A process according to claim 1 wherein the alcohol is selected from the group consisting of ethyl alcohol, isopropyl alcohol and tert-butylalcohol.

Claim 8

A process according to claim 1 wherein the catalyst is selected from the group consisting of palladium (II) chloride, palladium (II) sulfate, palladium (II) oxalate, palladium (II) acetate, palladium (II) iodide, copper (II) chloride, rhodium (III) chloride, and copper (I) iodide.

Claim 9

A process according to claim 7 wherein the catalyst is palladium (II) chloride.

Claim 10

A process according to claim 7 wherein the catalyst is copper (I) iodide.

Claim 11

A process according to claim 1 wherein the amine is selected from the group consisting of aniline, triethylamine, diethyl amine and 1,8-bis(dimethylamino) naphthalene.

Claim 12

A process according to claim 10 wherein the amine is triethylamine.

Claim 13

A process according to claim 1 wherein the pressure is between about 100 and 200 atmospheres and the temperature is in the range of about 100° to 125° C.

Claim 14

A process for the preparation of oxalate esters of an alcohol having from 1 to 20 carbon atoms which comprises reacting under substantially anhydrous conditions a saturated monohydric aliphatic or alicyclic alcohol which may contain other substituents which do not interfere with the reaction or an aromatic alcohol selected from the group consisting of benzyl, chlorobenzyl, and methoxy-benzyl alcohols with carbon monoxide at a pressure of between about 1 and 700 atmospheres and at a temperature in the range of about 50° to 250° C. in the presence of an effective amount of a catalyst selected from the group consisting of a palladium (II), rhodium (III), platinum (II) halide, sulfate, oxalate, or acetate and a copper (I) or copper (II) halide, at least a stoichiometric amount of an aliphatic, cycloaliphatic, aromatic or heterocyclic amine or ammonia, and at least a stoichiometric amount of an oxidant salt compound selected from the group consisting of a copper (II) or iron (III) oxalate, sulfate, acetate, or trifluroacetate, and recovering the desired oxalate ester.

Claim 15

A process for the preparation of oxalate esters of an alcohol having from 1 to 20 carbon atoms which comprises reacting under substantially anhydrous conditions a saturated monohydric aliphatic or alicyclic alcohol which may contain other substituents which do not interfere with the reaction or an aromatic alcohol selected from the group consisting of benzyl, chlorobenzyl, and methoxy-benzyl alcohols with carbon monoxide at a pressure of between about 1 and 700 atmospheres and at a temperature in the range of about 50° to 250° C. in the presence of an effective amount of a catalyst selected from the group consisting of a palladium (II), rhodium (III), platinum (II) halide, sulfate, oxalate, or acetate and a copper (I) or copper (II) halide, at least a stoichiometric amount of an aliphatic, cycloaliphatic, aromatic or heterocyclic amine or ammonia, and at least a stoichiometric amount of an oxidant salt compound selected from the group consisting of a copper (II) or iron (III) oxalate, sulfate, acetate, or trifluroacetate, and recovering the desired oxalate ester.

Claim 16

A process according to claim 13 wherein the pressure is between about 100 and 200 atmospheres and the temperature is in the range of about 100° to 125° C.

Claim 17

A process according to claim 13 wherein a triphenylphosphine, arsine or stibine ligand is added to the reaction mixture.

Claim 18

A process according to claim 13 wherein the alcohol is isopropyl alcohol, the catalyst is palladium (II) chloride, the amine is triethylamine and the oxidant salt compound is copper (II) sulfate.

Claim 19

A process according to claim 13 wherein the alcohol is ethyl alcohol, the catalyst is palladium (II) chloride, the amine is triethylamine and the oxidant salt compound is copper (II) sulfate.