Conversion of furfuryl alcohol into ethyl levulinate using solid acid catalysts
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Updated: Jun 23, 2026

A Novel Method for the Pentosan Analysis Present in Jute Biomass and Its Conversion into Sugar Monomers Using Acidic Ionic Liquid
Published on: June 1, 2018
Jean-Paul Lange1, Wouter D van de Graaf, René J Haan
1Shell Global Solutions, Shell Research and Technology Centre, Badhuisweg 3, Amsterdam, Netherlands. jean-paul.lange@shell.com
Abstract:
Furfural, a potential coproduct of levulinic acid, can be converted into levulinic acid via hydrogenation to furfuryl alcohol and subsequent ethanolysis to ethyl levulinate. The ethanolysis reaction is known to proceed in the presence of H(2)SO(4). We show here that several strongly acidic resins are comparably effective catalysts for this reaction. Optimal performance is achieved by balancing the number of acid sites with their accessibility in the resin. Acidic zeolites such as H-ZSM-5 also catalyze this reaction, although with a lower activity and a higher co-production of diethyl ether.
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