Direct Transformation of HMF into 2,5-Diformylfuran and 2,5-Dihydroxymethylfuran without an External Oxidant or Reductant

Abstract

The selective transformation of 5-hydroxymethylfurfural (HMF) to valuable 2,5-diformylfuran (DFF) and 2,5-dihydroxymethylfuran (DHMF) is highly desirable but remains a great challenge owing to its tendency to over-oxidation and over-reduction. In this work, HMF is directly converted into DFF and DHMF without external oxidant or reductant through a Meerwein-Ponndorf-Verley-Oppenauer (MPVO) reaction. In such a MPVO process, HMF is used as both oxidant and reductant and DFF and DHMF are simultaneously produced with a 1:1 molar ratio in the presence of a Lewis acid catalyst. Under high initial HMF concentration, a HMF conversion of up to 44.7 % can be reached within 1 h. Moreover, this atom-efficient transformation route for HMF also provides a promising protocol for the crude separation of DHMF products from DFF products, owing to the lower solubility of DHMF compared to DFF in acetonitrile.

Keywords: 5-hydroxymethylfurfural; biomass conversion; lewis acid; oxidation; reduction.