An unexpected highly diastereoselective double Baylis–Hillman reaction of per- (or poly)fluorophenyl aromatic aldimines with methyl vinyl ketone

Aza-Baylis–Hillman reaction of per- (or poly)fluorophenyl aromatic aldimines with methyl vinyl ketone (MVK) was studied. It was found that both the used Lewis base and solvent can significantly affect the reaction. Using triphenylphosphine as a Lewis base, the reaction of with MVK proceeded smoothly to give the normal Baylis–Hillman adduct along with the double Baylis–Hillman adduct as by-product in THF. When 1,4-diazabicyclo[2.2.2]octane was used as a Lewis base in DMF, the aza-Baylis–Hillman reaction of with MVK gave the double aza-Baylis–Hillman adduct exclusively in moderate to good yields with excellent diastereoselectivities. The double Baylis–Hillman adduct was conveniently converted to fluorine-containing 4-alkylidene-2-cyclohexen-1-ones under mild reaction conditions in good yields.