TCCA/PhSH-Mediated regioselective hydroethoxylation and hydromethoxylation of allenamides via a radical process.

Abstract

An efficient TCCA/PhSH-mediated regioselective hydroethoxylation and hydromethoxylation of allenamides via a radical process was developed to create a workable route to γ-oxygenated enamides. This process is highly regioselective, affording (E)-γ-oxygenated enamides in moderate to good yields. Mechanistic investigations indicated that the ethoxy radical was formed through the motivation of TCCA/PhSH, which subsequently added to the terminal carbon of allenamides to form the vinyl radical intermediate. The efficiency of the gram-scale reaction suggests the potential industrial application of this synthetic method. Notably, our approach eliminates the need for metal catalysts representing a significant advancement in greener chemistry practices.