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Acid-catalyzed hydrolysis of ring-substituted phenyl vinyl sulfides

โœ Scribed by T. Okuyama; M. Masago; M. Nakada; T. Fueno

Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
351 KB
Volume
33
Category
Article
ISSN
0040-4020

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Terminal vinyl and chlorovinyl sulfides are hydrolyzed by 70% perchloric acid-thiophenol in benzene to the corresponding diphenyl thioacetals and thioesters in good yields. Vinyl sulfides are very important class of compounds due to their versatility in organic synthesisl. Numerous methods are avail