Electrochemical benzylic oxidation of C-H bonds
Jason A Marko1, Anthony Durgham, Stacey Lowery Bretz
1Department of Chemistry and Biochemistry, Miami University, Oxford, Ohio, 45056, USA. wei.liu@miamioh.edu.
Abstract:
Oxidized products have become increasingly valuable as building blocks for a wide variety of different processes and fine chemistry, especially in the benzylic position. We report herein a sustainable protocol for this transformation through C-H functionalization and is performed using electrochemistry as the main power source and tert-butyl hydroperoxide as the radical source for the C-H abstraction. The temperature conditions reported here do not increase above 50 °C and use an aqueous-based medium. A broad substrate scope is explored, along with bioactive molecules, to give comparable and increased product yields when compared to prior reported literature without the use of electrochemistry.
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