Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1313797 | Journal of Fluorine Chemistry | 2014 | 6 Pages |
•Preparation of N-difluoromethylimidazoles and benzimidazoles.•Use of fluoroform as a source of difluorocarbene.•Preparation of difluoromethoxypyridines.
Fluoroform is used as a source of difluorocarbene to convert various N-, O-, and C-nucleophiles to their difluoromethylated derivatives. Imidazole, benzimidazole, benztriazole, hydroxypyridines, and their derivatives underwent reaction at moderate temperatures and atmospheric pressure, using potassium hydroxide as base in a two-phase (water/acetonitrile) process to provide moderate to good yields of the respective products. Nitrophenols required addition of a co-solvent (methanol) to obtain good yields of products.
Graphical abstractDifluorocarbene source, CHF3, can be used as a diverse difluoromethylating agent.Figure optionsDownload full-size imageDownload as PowerPoint slide