Issue 54, 2018

Efficient conversion of 5-hydroxymethylfurfural to high-value chemicals by chemo- and bio-catalysis

Abstract

5-hydroxymethylfurfural (HMF) is a very important versatile platform compound derived from renewable biomass. The functionalized molecule with an aldehyde group, a hydroxyl group and a furan ring provides great potential for the production of a wide variety of valuable chemicals. This review highlights the latest advances in the catalytic conversion of HMF into value-added chemicals by some important reactions including (1) aerobic oxidation of HMF into furan-based aldehydes and acids such as 5-hydroxymethyl-2-furancarboxylic acid (HMFCA), 2,5-diformylfuran (DFF), and furandicarboxylic acid (FDCA), (2) reductive amination of HMF to amine, (3) the synthesis of aromatics by Diels–alder reaction followed by a dehydration reaction, (4) catalytic reduction of HMF into 2,5-bis(hydroxymethyl)furan (BHMF), and 2,5-dimethyl furan (DMF), (5) catalytic oxidation of HMF into maleic anhydride, and some other important transformations. The review mainly focuses on the recent progress in bio-catalytic, electrocatalytic, and heterogeneous catalytic transformation of HMF into high value chemicals over the past few years. Moreover, an outlook is provided to highlight opportunities and challenges related to this hot research topic.

Graphical abstract: Efficient conversion of 5-hydroxymethylfurfural to high-value chemicals by chemo- and bio-catalysis

Article information

Article type
Review Article
Submitted
21 Jūn. 2018
Accepted
28 Aug. 2018
First published
03 Sept. 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 30875-30886

Efficient conversion of 5-hydroxymethylfurfural to high-value chemicals by chemo- and bio-catalysis

H. Xia, S. Xu, H. Hu, J. An and C. Li, RSC Adv., 2018, 8, 30875 DOI: 10.1039/C8RA05308A

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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