Issue 27, 2022

The copper-catalyzed oxidation of arylmethyl triazines with H2O toward the oxidant-free synthesis of aroyl triazines

Abstract

We report an efficient copper-catalyzed dehydrogenation method for the synthesis of aroyl triazines from arylmethyl triazines with water in the absence of additional oxidants or hydrogen acceptors. The use of substrates with both electron-donating and electron-withdrawing groups resulted in moderate to good yields. Using liquid chromatography–mass spectrometry, 18O-labeled-water reactions and hydrogen capture experiments confirmed that water was the only oxygen donor and hydrogen was the by-product. This oxidation strategy provides a new approach for the synthesis of aroyl triazines with a broad substrate scope.

Graphical abstract: The copper-catalyzed oxidation of arylmethyl triazines with H2O toward the oxidant-free synthesis of aroyl triazines

Supplementary files

Article information

Article type
Paper
Submitted
28 Mar 2022
Accepted
25 Apr 2022
First published
26 Apr 2022

Org. Biomol. Chem., 2022,20, 5406-5411

The copper-catalyzed oxidation of arylmethyl triazines with H2O toward the oxidant-free synthesis of aroyl triazines

M. Zeng, Z. Yuan, L. Wen, D. Jiang, H. Lu, W. Liu, J. Dai and S. Zeng, Org. Biomol. Chem., 2022, 20, 5406 DOI: 10.1039/D2OB00582D

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