116432-92-9Relevant academic research and scientific papers
Metal-free C-H thioarylation of arenes using sulfoxides: A direct, general diaryl sulfide synthesis
Fernández-Salas, José A.,Pulis, Alexander P.,Procter, David J.
, p. 12364 - 12367 (2016/10/22)
Metal-free C-H thioarylation of arenes and heteroarenes using methyl sulfoxides constitutes a general protocol for the synthesis of high value diaryl sulfides. The coupling of arenes and heteroarenes with in situ activated sulfoxides is regioselective, uses readily available starting materials, is operationally simple, and tolerates a wide range of functional groups.
Lewis Acid Catalyzed Sulphenylation of Methylbenzene by p-Chlorobenzenesulphenyl Chloride
Grant, Douglas W.,Hogg, Donald R.,Wardell, James L.
, p. 3123 - 3143 (2007/10/02)
The Lewis acid catalyzed reactions of benzene and several methylbenzenes with p-chlorobenzenesulphenyl chloride are reported.The products include sulphenylated arenes - p-chlorophenyl aryl sulphides, bis(p-chlorophenylthio)arenes, chloro(p-chlorophenylthio)arenes - as well as chlorinated arenes and bis(p-chlorophenyl)disulphides.The disulphide: combined sulphenylation products ratio for each arene, e.g. 27:73 (for benzene) and 12:86 (for mesitylene), shows only a small variation when compared to the large differences in reactivity of the arenes towards electrophilic reagents.
