Recyclable Oxofluorovanadate‐Catalyzed Formylation of Amines by Reductive Functionalization of CO₂ with Hydrosilanes

Abstract

An efficient method has been developed for the reductive amination of CO₂ by using readily available and recyclable oxofluorovanadates as catalysts. Various amines are transformed into the desired N-formylated products in moderate to excellent yields at room temperature in the presence of phenylsilane. Mechanistic studies based on in situ infrared spectroscopy suggest a reaction pathway initiated through F-Si interactions. The activated phenylsilane allows for CO₂ insertion to produce phenylsilyl formate, which undergoes attack by the amine to generate the target product.