Issue 66, 2017, Issue in Progress

Dehydration of glucose to 5-hydroxymethylfurfural and 5-ethoxymethylfurfural by combining Lewis and Brønsted acid

Abstract

In this work, glucose was transformed into 5-hydroxymethylfurfural (HMF) and 5-ethoxymethylfurfural (EMF) in the presence of AlCl3·6H2O and a Brønsted solid acid catalyst (PTSA–POM). GVL (γ-valerolactone)–water and ethanol–water solvent systems were evaluated in the dehydration reaction of glucose into HMF and EMF, respectively. Water content and dosage of AlCl3·6H2O were examined in the conversion of glucose into HMF, and some valuable chlorides (FeCl3·6H2O, NiCl2·6H2O, CrCl3·6H2O etc.) were also used in contrast with AlCl3·6H2O. Some different organic solvents were added to the ethanol–water system to explore whether it would be beneficial to the generation of EMF. A high yield of HMF (60.7%) was obtained at 140 °C within 60 min in GVL–water (10 : 1) solvent system, and total yield 42.1% of EMF and HMF (30.6% EMF, 11.5% HMF) was achieved at 150 °C after 30 min in an ethanol–water (9 : 1) solvent system.

Graphical abstract: Dehydration of glucose to 5-hydroxymethylfurfural and 5-ethoxymethylfurfural by combining Lewis and Brønsted acid

Article information

Article type
Paper
Submitted
13 Jul 2017
Accepted
19 Aug 2017
First published
25 Aug 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 41546-41551

Dehydration of glucose to 5-hydroxymethylfurfural and 5-ethoxymethylfurfural by combining Lewis and Brønsted acid

H. Xin, T. Zhang, W. Li, M. Su, S. Li, Q. Shao and L. Ma, RSC Adv., 2017, 7, 41546 DOI: 10.1039/C7RA07684C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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