Thioethers from Halogen Compounds and Cuprous Mercaptides. II

R Adams, A Ferretti

Index: Adams; Ferretti Journal of the American Chemical Society, 1959 , vol. 81, p. 4927,4929

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Citation Number: 102

Abstract

The reaction of aliphatic cuprous mercaptides with various halogen compounds has been further explored. Aliphatic and aromatic thioethers have been formed by condensation of cuprous niercaptides with 2-bromothiophene, 2-bromopyridine and 2-broniofuroic acid, the last with concomitant decarboxylation. P-Bromostyrene, 1-bromo-2-methyl-1-propene and 1- chloro-or 1-bromo-dodecane represent prototypes of other halogen compounds which ...