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. 2020 Aug 19;56(66):9509-9512.
doi: 10.1039/d0cc03695a.

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

Lisa Goclik  1 , Lisa Offner-Marko  1 , Alexis Bordet  2 , Walter Leitner  1
Affiliations

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

Lisa Goclik et al. Chem Commun (Camb). .

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.

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