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Herein, 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.
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Oliver P. Williams
Alyah F. Chmiel
Myriam Mikhael
Angewandte Chemie International Edition
University of Wisconsin–Madison
Merck & Co., Inc., Rahway, NJ, USA (United States)
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Williams et al. (Sat,) studied this question.
www.synapsesocial.com/papers/69de7ba56e50a6aba3e93c0d — DOI: https://doi.org/10.1002/anie.202300178
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