Synthesis and reactivity of benzylic sulfonium salts: benzylation of phenol and thiophenol under near-neutral conditions

Abstract

A series of benzyldimethylsulfonium - and related hydrogensulfate salts have been synthesized from the ternary system ArCH 2OH:H 2SO 4: Me 2S or tetrahydrothiophene. The salts are generally stable crystalline solids, but anomalously high reactivity is observed for 9-(anthrylmethyl)dimethylsulfonium hydrogensulfate. Selected sulfonium salts have been used for the O- and S-benzylation of phenol and thiophenol, respectively, in a two phase system under near-neutral conditions. The benzylation of oximes and benzimidazole under basic conditions is also described.