Issue 37, 2024, Issue in Progress

TsOH-catalyzed dehydroxylative cross-coupling of alcohols with phenols: rapid access to propofol derivatives

Abstract

Modification of the parent structure of molecules often alters their physicochemical properties and biological activities. Herein, a practical, efficient, and highly regioselective C–H alkylation of phenols with alcohols via dehydroxylative cross-coupling was developed to produce para-alkylated phenols with excellent regioselectivities and yields, using which propofol derivatives were rapidly synthesized. This process is performed under mild and simple conditions and is well-compatible with a variety of alcohols (secondary and tertiary benzylic alcohols as well as allyl alcohols) as alkylated agents. In addition, high aryl ether derivatives were also obtained using this catalytic system.

Graphical abstract: TsOH-catalyzed dehydroxylative cross-coupling of alcohols with phenols: rapid access to propofol derivatives

Supplementary files

Article information

Article type
Paper
Submitted
27 Jun 2024
Accepted
04 Aug 2024
First published
23 Aug 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 26857-26862

TsOH-catalyzed dehydroxylative cross-coupling of alcohols with phenols: rapid access to propofol derivatives

Y. Liang, C. Liu, Y. Li and L. Ouyang, RSC Adv., 2024, 14, 26857 DOI: 10.1039/D4RA04674A

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