Issue 66, 2020

Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu@SILP catalyst

Abstract

The selective hydrodeoxygenation of hydroxyacetophenone derivatives is achieved opening a versatile pathway for the production of valuable substituted ethylphenols from readily available substrates. Bimetallic iron ruthenium nanoparticles immobilized on an imidazolium-based supported ionic liquid phase (Fe25Ru75@SILP) show high activity and stability for a broad range of substrates without acidic co-catalysts.

Graphical abstract: Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu@SILP catalyst

Supplementary files

Article information

Article type
Communication
Submitted
25 May 2020
Accepted
13 Jul 2020
First published
16 Jul 2020
This article is Open Access
Creative Commons BY license

Chem. Commun., 2020,56, 9509-9512

Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu@SILP catalyst

L. Goclik, L. Offner-Marko, A. Bordet and W. Leitner, Chem. Commun., 2020, 56, 9509 DOI: 10.1039/D0CC03695A

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