Issue 30, 2023

Efficient synthesis of ynones from carboxylic acids and terminal alkynes via Pd/Cu catalysis using 2-chloroimidazolium chloride as the activation reagent

Abstract

In this work, we have developed a successful Sonogashira coupling reaction utilizing IPrCl-Cl as the activation reagent to couple carboxylic acids with terminal alkynes. The reaction employs CuI/Pd(PPh3)2Cl2 as the co-catalyst and Et3N as the solvent, resulting in excellent yields (up to 88%) of ynones. The use of carboxylic acids as a starting material makes this method a valuable contribution to organic synthesis.

Graphical abstract: Efficient synthesis of ynones from carboxylic acids and terminal alkynes via Pd/Cu catalysis using 2-chloroimidazolium chloride as the activation reagent

Supplementary files

Article information

Article type
Paper
Submitted
20 May 2023
Accepted
26 Jun 2023
First published
27 Jun 2023

New J. Chem., 2023,47, 14374-14379

Efficient synthesis of ynones from carboxylic acids and terminal alkynes via Pd/Cu catalysis using 2-chloroimidazolium chloride as the activation reagent

W. Zheng, N. Liang, Y. Fu, J. Zhong, Y. Zhang, L. Wang, Y. Wang and Q. Wang, New J. Chem., 2023, 47, 14374 DOI: 10.1039/D3NJ02316H

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