Union Carbide Chemicals & Plastics Technology Corporation

Union Carbide Chemicals and Plastics Company, Inc.

Jonathan Joshua Kurland

Bruce Armin Barner

John Robert Briggs

William G Etzkorn

Gordon G Harkreader

Donald Leroy Bunning

Ernesto Vera-Castaneda

William M Haydon

Wai C Liu

Bruce A Barner

Charles G Moyers, Jr

This invention relates to a process for preparing carboxylic acids by oxidizing an aldehyde with a peracid in the presence of an amine and/or amine N-oxide catalyst selected from the group consisting of a substituted or unsubstituted alkyl amine, alkyl amine N-oxide, aromatic amine, aromatic amine N-oxide, heterocyclic amine, heterocyclic amine N-oxide and mixtures thereof, to produce the carboxylic acid. Such carboxylic acids have utility for example as chemical intermediates.

Process for preparing carboxylic acids

This invention relates to a process for preparing optically active carboxylic acids by oxidizing an optically active aldehyde with a peracid in the presence of an amine and/or amine N-oxide catalyst selected from the group consisting of a substituted or unsubstituted alkyl amine, alkyl amine N-oxide, aromatic amine, aromatic amine N-oxide, heterocyclic amine, heterocyclic amine N-oxide and mixtures thereof, to produce the optically active carboxylic acid. Such optically active carboxylic acids have utility for example as pharmaceuticals.

Process for preparing optically active carboxylic acids

The present invention relates to a process for producing an optically active aldehyde (first aldehyde) containing a reduced amount of the corresponding enantiomeric aldehyde (second aldehyde) which process comprises: (1) providing an initial solution containing a non-eutectic mixture of the first aldehyde and the second aldehyde, which mixture has a composition in the compositional region where only the first aldehyde crystallizes when its solubility limit in the solution is exceeded, and (2) maintaining the solution at a temperature above the eutectic temperature of the mixture and under conditions such that the solubility limit of the first aldehyde is exceeded so as to form a crystalline first aldehyde containing relatively less of the second aldehyde than was present in the initial solution.

Process for improving enantiomeric purity of aldehydes

This invention relates to a method for removing halides from liquid carboxylic acid contaminated with a halide impurity by contacting the liquid halide-contaminated acid with a silver(I)-exchanged macroreticular resin. The halide reacts with the resin-bound silver and is removed from the carboxylic acid stream. The present invention also relates to an improved method for producing silver-exchanged macroreticular resins suitable for use in the present invention.

Process for preparing silver(I)-exchanged resins

A process for producing acrylic ester by the catalytic esterification of a crude liquid stream of enriched acrylic acid recovered by the partial condensation of the reaction gas effluent from the catalytic oxidation of propylene and/or acrolein. The partial condensation allows a significant proportion of volatile aldehydes and water to pass through the first recovery stage to a second stage for conventional recovery, along with uncondensed acrylic acid vapors and the remainder of the uncondensed reaction gases.

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Charleston, WV, United States of America

Jonathan Joshua Kurland