68121-46-0Relevant articles and documents
Copper-Catalyzed Methylthiolation of Aryl Iodides and Bromides with Dimethyl Disulfide in Water
Wang, Ying-Yu,Wu, Xiang-Mei,Yang, Ming-Hua
supporting information, (2020/07/20)
An efficient route to aryl methyl sulfides through the copper-catalyzed coupling reaction of aryl iodides or bromides with dimethyl disulfide in water is described. Electron-donating and electron-withdrawing functional groups in the substrates were tolerated, and the corresponding products were obtained in moderate to good yields.
Efficient synthesis of aryl methyl sulfide derivatives using (methylthio)trimethylsilane as methylthiolation reagent
Qiao, Qi,Dominique, Romyr,Sidduri, Achyutharao,Lou, Jianping,Goodnow, Robert A.
scheme or table, p. 3691 - 3698 (2010/12/25)
The synthesis of various aryl methyl sulfides has been achieved by treatment of nitroarenes with a combination of (methylthio)trimethylsilane and cesium carbonate in dimethylsulfoxide. This reaction gives access to aryl methyl sulfide derivatives in high yields. Copyright
Nonaqueous diazotization of arylamines in the presence of dimethyldisulfide; the convenient synthesis of arylmethylsulfides from anilines
Allaire,Lyga
, p. 1857 - 1861 (2007/10/03)
Modest to good isolated yields of arylmethylsulfides are obtained by the reaction of anilines with alkylnitrite under nonaqueous conditions in the presence of 0.5 molar equivalents of dimethyldisulfide.