Article ID Journal Published Year Pages File Type
1314024 Journal of Fluorine Chemistry 2015 9 Pages PDF
Abstract

•The dibromofluoromethylation of aryl Grignard reagents was developed.•The reaction proceeded via a difluorocarbene-mediated mechanism.•α,α-Dibromo-α-fluorotoluene derivatives were obtained.

The dibromofluoromethylation of aryl Grignard reagents bearing electron-withdrawing groups with dibromodifluoromethane (CF2Br2) proceeded in the presence of LiBr. The reaction gave the corresponding α,α-dibromo-α-fluorotoluene derivatives through halogen exchange reaction of intermediate difluorobenzyl anions.

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Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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