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Electrochemical hydrogenation of α-ketoesters and benzoxazinones using carbon electrodes and a sustainable Brønsted acid†
Dion B. Nemez,Baldeep K. Sidhu,Patrick K. Giesbrecht,Jason D. Braun,David E. Herbert
Organic Chemistry Frontiers Pub Date : 11/26/2020 00:00:00 , DOI:10.1039/D0QO01311K
Abstract

The direct electrochemical hydrogenation of unsaturated organic compounds containing C[double bond, length as m-dash]N and C[double bond, length as m-dash]O bonds using glassy carbon electrodes and a widely available Brønsted acid is demonstrated for a selection of α-ketoesters and benzoxazinones. In this simple set-up, the reduced products are formed with excellent selectivity, without the use of a redox mediator, and are easily recovered in good yields by extraction. The carbon-based electrode is essential to the observation of the hydrogenated product; no turnover is observed using platinum mesh.

Graphical abstract: Electrochemical hydrogenation of α-ketoesters and benzoxazinones using carbon electrodes and a sustainable Brønsted acid
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