Issue 0, 1967

The reaction of phenylacetonitrile with carbon disulphide and the preparation of 4-aryl isothiazoles

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.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 124-124

The reaction of phenylacetonitrile with carbon disulphide and the preparation of 4-aryl isothiazoles

M. Davis, G. Snowling and R. W. Winch, J. Chem. Soc. C, 1967, 124 DOI: 10.1039/J39670000124

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