Hydrocyclization/Defluorination of CF₃‐Substituted Acrylamides: Insights from Kinetics of Hydrogen Atom Transfer

The introduction of F-containing groups into organic molecules can significantly alter their physical and chemical properties. Particularly, gem-difluoroalkenes serve as versatile precursors for a broad variety of organofluorine compounds, commonly used in agrochemicals, pharmaceuticals, and materials science. Based on the kinetics of H• transfer to acrylamide (k_H = 2.28 × 10^-4 M^-1 s^-1 at 300 K in toluene), the study describes a nickel-hydride-(or Li[BEt₃H]) initiated hydrocyclization/defluorination of CF₃-substituted acrylamides, offering alternative access to 4-fluorovinyl-substituted 2-pyrrolidones (Seletracetam derivatives that are antiepileptic drug candidates). This process proceeds with high yields and remarkable chemo- and regioselectivity. The hydrocyclization/defluorination can be initiated by either H• or H^- transfer, followed by a 5-exo-trig cyclization and subsequent fluorine elimination. The strategy has been applied in the late-stage functionalization of drug molecules, providing a valuable tool in the synthesis of pharmaceutical compounds.