Current Advances in the Sustainable Conversion of 5-Hydroxymethylfurfural into 2,5-Furandicarboxylic Acid

ChemSusChem. 2022 Jul 7;15(13):e202200501. doi: 10.1002/cssc.202200501. Epub 2022 May 13.

Abstract

2,5-Furandicarboxylic acid (FDCA) is currently considered one of the most relevant bio-sourced building blocks, representing a fully sustainable competitor for terephthalic acid as well as the main component in green polymers such as poly(ethylene 2,5-furandicarboxylate) (PEF). The oxidation of biobased 5-hydroxymethylfurfural (HMF) represents the most straightforward approach to obtain FDCA, thus attracting the attention of both academia and industries, as testified by Avantium with the creation of a new plant expected to produce 5000 tons per year. Several approaches allow the oxidation of HMF to FDCA. Metal-mediated homogeneous and heterogeneous catalysis, metal-free catalysis, electrochemical approaches, light-mediated procedures, as well as biocatalytic processes share the target to achieve FDCA in high yield and mild conditions. This Review aims to give an up-to-date overview of the current developments in the main synthetic pathways to obtain FDCA from HMF, with a specific focus on process sustainability.

Keywords: 2,5-furandicarboxylic acid; biocatalysis; electrocatalysis; heterogeneous catalysis; photocatalysis.

Publication types

  • Review

MeSH terms

  • Dicarboxylic Acids*
  • Furaldehyde* / analogs & derivatives
  • Furaldehyde* / metabolism
  • Furans / metabolism

Substances

  • Dicarboxylic Acids
  • Furans
  • 5-hydroxymethylfurfural
  • 2,5-furandicarboxylic acid
  • Furaldehyde