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The reaction of phenylacetonitrile with carbon disulphide and the preparation of 4-aryl isothiazoles
Journal of the Chemical Society C: Organic Pub Date : , DOI:10.1039/J39670000124
Abstract

Dithioacid salts have been prepared in good yield from phenylacetonitrile and related compounds by reaction with carbon disulphide in benzene solution using sodium hydride as the base; substituted isothiazoles are formed on heating these salts, in ethanol solution, with sulphur.

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