Affiliation:
1. Department of Chemistry University of Wisconsin-Madison Madison WI-53706 USA
2. Discovery Chemistry Merck & Co., Inc. 33 Avenue Louis Pasteur Boston MA-02115 USA
Abstract
AbstractHerein, we describe a practical protocol for the removal of alcohol functional groups through reductive cleavage of their benzoate ester analogs. This transformation requires a strong single electron transfer (SET) reductant and a means to accelerate slow fragmentation following substrate reduction. To accomplish this, we developed a photocatalytic system that generates a potent reductant from formate salts alongside Brønsted or Lewis acids that promote fragmentation of the reduced intermediate. This deoxygenation procedure is effective across structurally and electronically diverse alcohols and enables a variety of difficult net transformations. This protocol requires no precautions to exclude air or moisture and remains efficient on multigram scale. Finally, the system can be adapted to a one‐pot benzoylation‐deoxygenation sequence to enable direct alcohol deletion. Mechanistic studies validate that the role of acidic additives is to promote the key C(sp3)−O bond fragmentation step.
Funder
National Institutes of Health