Indium trifluoride: A highly efficient catalyst for the synthesis of fluorine-containing 2,4,5-trisubstituted imidazoles under solvent-free conditions

A new green protocol has been developed for the synthesis of fluorine containing 2,4,5-trisubstituted imidazoles via one-pot, three-component condensation reaction of 4,4-difluorobenzil with aldehydes and ammonium acetate using reusable indium (III) fluoride (InF3) as Lewis acid catalyst under solvent-free conditions. This protocol provides a novel and improved method for obtaining fluorine containing 2,4,5-trisubstituted imidazoles in terms of good yields with little catalyst loading.

An efficient and one-pot protocol for the synthesis of fluorine-containing 2,4,5-trisubstituted imidazoles promoting by InF3 under solvent-free conditions is described.Figure optionsDownload as PowerPoint slideHighlights
► Fluorine-containing 2,4,5-trisubstituted imidazoles are synthesized from one-pot reactions.
► The reactions are promoted efficiently by indium (III) fluoride.
► The reactions are undergoing in solvent-free conditions.
► The catalyst can be recycled and reused.
► The methodology tolerates most of substrates.