Issue 5, 2017

Copper-catalyzed aromatic C–H alkoxylation with alcohols under aerobic conditions

Abstract

An efficient protocol for copper-catalyzed aromatic C–H alkoxylation with alcohols has been developed under aerobic conditions. The protocol provides a complementary method to couple arenes and alcohols to furnish aromatic ethers. The advantages of this method are the employment of a cheap Cu(OAc)2 catalyst, oxygen as the terminal oxidant and alcohol as both an alkoxy reagent and a solvent. Notably, the catalytic amount of benzoic acid plays a significant role in this transformation.

Graphical abstract: Copper-catalyzed aromatic C–H alkoxylation with alcohols under aerobic conditions

Supplementary files

Article information

Article type
Paper
Submitted
25 Nov 2016
Accepted
05 Jan 2017
First published
05 Jan 2017

Org. Biomol. Chem., 2017,15, 1261-1267

Copper-catalyzed aromatic C–H alkoxylation with alcohols under aerobic conditions

W. Lu, H. Xu and Z. Shen, Org. Biomol. Chem., 2017, 15, 1261 DOI: 10.1039/C6OB02582J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements