Synthesis of Bis(hydroxylmethylfurfuryl)amine Monomers from 5-Hydroxymethylfurfural

ChemSusChem. 2016 Jun 8;9(11):1255-8. doi: 10.1002/cssc.201600122. Epub 2016 May 6.

Abstract

We report the synthesis of bis(hydroxylmethylfurfuryl)amine (BHMFA) from 5-hydroxymethylfurfural (5-HMF) by reacting 5-HMF with primary amines in the presence of homogeneous Ru(II) catalysts having sterically strained ligands. BHMFA is a group of furan-based monomers that offer great potential to form functional biopolymers with tunable properties. A range of primary amines, such as aliphatic and benzyl amines, are readily converted with 5-HMF to form the corresponding BHMFA in good yields. The reaction proceeds through reductive amination of 5-HMF with primary amine to form secondary amine, followed by reductive amination of 5-HMF with in situ generated secondary amine to produce BHMFA.

Keywords: biomass; green chemistry; polymers; renewable resources; ruthenium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemical synthesis*
  • Amines / chemistry*
  • Catalysis
  • Chemistry Techniques, Synthetic
  • Furaldehyde / analogs & derivatives*
  • Furaldehyde / chemistry
  • Furans / chemical synthesis*
  • Furans / chemistry*
  • Hydrogenation
  • Ruthenium / chemistry

Substances

  • Amines
  • Furans
  • 5-hydroxymethylfurfural
  • Ruthenium
  • Furaldehyde