Issue 3, 2022

H2O2-mediated room temperature synthesis of 2-arylacetophenones from arylhydrazines and vinyl azides in water

Abstract

An environmentally benign, cost-efficient and practical methodology for the room temperature synthesis of 2-arylacetophenones in water has been discovered. The facile and efficient transformation involves the oxidative radical addition of arylhydrazines with α-aryl vinyl azides in the presence of H2O2 (as a radical initiator) and PEG-800 (as a phase-transfer catalyst). From the viewpoint of green chemistry and organic synthesis, the present protocol is of great significance because of using cheap, non-toxic and readily available starting materials and reagents as well as amenability to gram-scale synthesis, which provides an attractive strategy to access 2-arylacetophenones.

Graphical abstract: H2O2-mediated room temperature synthesis of 2-arylacetophenones from arylhydrazines and vinyl azides in water

Supplementary files

Article information

Article type
Paper
Submitted
15 Oct 2021
Accepted
14 Dec 2021
First published
22 Dec 2021

Org. Biomol. Chem., 2022,20, 630-635

H2O2-mediated room temperature synthesis of 2-arylacetophenones from arylhydrazines and vinyl azides in water

M. Luo, Y. Zhang, P. Fang, Y. Li, C. Qi, Y. Li, R. Shen, K. Cheng and H. Wang, Org. Biomol. Chem., 2022, 20, 630 DOI: 10.1039/D1OB02023D

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