Issue 43, 2024

Alkoxyhydrosilane-facilitated cross-etherification reaction of secondary benzyl alcohol with aliphatic alcohol: synthesis of unsymmetrical dialkyl ethers

Abstract

Alkoxyhydorosilane is found to be an effective mediator for the cross-etherification reaction between two distinct alcohols, namely, a secondary benzyl alcohol and an aliphatic alcohol, providing the unsymmetrical dialkyl ethers in good-to-high yields. The reaction is also successfully applied to the lignin model compound, which is an important renewable non-fossil organic carbon source. Initial mechanistic studies indicated that the carbocation derived from benzyl alcohol was formed under the present reaction conditions.

Graphical abstract: Alkoxyhydrosilane-facilitated cross-etherification reaction of secondary benzyl alcohol with aliphatic alcohol: synthesis of unsymmetrical dialkyl ethers

Supplementary files

Article information

Article type
Paper
Submitted
19 Aug 2024
Accepted
26 Sep 2024
First published
04 Oct 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 31467-31470

Alkoxyhydrosilane-facilitated cross-etherification reaction of secondary benzyl alcohol with aliphatic alcohol: synthesis of unsymmetrical dialkyl ethers

T. Hashimoto, Y. Matsunaga, Y. Okamura, S. Takao and M. Hojo, RSC Adv., 2024, 14, 31467 DOI: 10.1039/D4RA05997B

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