Magnesium mediated preparation of fluorinated alkyl silanes
AssigneeUniversity of Southern California
InventorsG.K. Surya Prakash, Jinbo Hu, George A. Olah
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Abstract
An efficient method is disclosed for the preparation of trifluoromethyl- and difluoromethylsilanes using magnesium metal mediated reductive tri- and difluoromethylation of chlorosilanes with tri- and difluoromethyl sulfides, sulfoxides, and sulfones. One byproduct of the process is diphenyl disulfide. Since phenyl trifluoromethyl sulfone, sulfoxide and sulfide are readily prepared from readily available trifluoromethane and diphenyl disulfide, the method can be considered “pseudo-catalytic” for the preparation of (trifluoromethyl)trimethylsilane from environmentally benign trifluoromethane.
Claims14
A method for preparing fluorinated alkyl silanes which comprises reacting a fluorinated alkyl sulfur containing compound with a silyl chloride in the presence of a reducing agent under reaction conditions sufficient to prepare a fluorinated alkyl silane.
Dependencies are inferred from the claim text.