Flow‐Enabled, Modular Access to α,α‐Difluoromethylene Amines

Abstract The α,α‐difluoromethylene amine (NCF 2 R) motif represents a useful functionality in medicinal chemistry, yet practical and modular methods to access this class of compounds are lacking. Here, we report a safe and scalable flow‐based strategy for the on‐demand generation of NCF 2 R anions using a packed‐bed microreactor containing caesium fluoride. This protocol enables the late‐stage installation of the CF 2 group under mild conditions, avoiding the use of hazardous fluorinating agents and minimizing fluorinated waste. This fully modular strategy features three points of diversification (carboxylic acid, sulfonamide, and electrophile), allowing efficient access to a broad range of α,α‐difluoromethylene amines. The method tolerates a variety of functional groups, supports late‐stage functionalization of pharmaceutically relevant scaffolds, and is compatible with downstream cross‐coupling reactions, demonstrating the robustness of the reaction protocol. This work provides a versatile platform for the streamlined incorporation of NCF 2 motifs, expanding the range of synthetic strategies available in medicinal and fluorine chemistry.