Volume 21, Issue 1 pp. 97-101
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bis-alkylsulfonylpyridines

S. G. Woods

S. G. Woods

Western Applied Sciences and Technology Laboratories, Dow Chemical U.S.A., 2800 Mitchell Drive, Walnut Creek, California 94598

Brigham Young University, Provo, UT 84601.

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B. T. Matyas

B. T. Matyas

Western Applied Sciences and Technology Laboratories, Dow Chemical U.S.A., 2800 Mitchell Drive, Walnut Creek, California 94598

Summer Student Trainee, 1979.

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A. P. Vinogradoff

A. P. Vinogradoff

Western Applied Sciences and Technology Laboratories, Dow Chemical U.S.A., 2800 Mitchell Drive, Walnut Creek, California 94598

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Y. C. Tong

Y. C. Tong

Western Applied Sciences and Technology Laboratories, Dow Chemical U.S.A., 2800 Mitchell Drive, Walnut Creek, California 94598

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First published: January/February 1984
Citations: 12

Abstract

Dihalogenated pyridines, some activated with carboxylic, ester or cyano group, were allowed to react with sodium alkylmercaptides. After hydrolysis of the ester or cyano group followed by decarboxylation, bis-alkylthiopyridines with substituents at 2,3-, 2,4-, 2,5-, 2,6- and 3,5-positions were prepared. These compounds were oxidized to bis-alkylsulfonylpyridines.

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