A gram scale selective oxidation of 5-hydroxymethylfurfural to diformylfuran in the presence of oxone and catalyzed by 2-iodobenzenesulfonic acid - Université de technologie de Compiègne Access content directly
Journal Articles New Journal of Chemistry Year : 2020

A gram scale selective oxidation of 5-hydroxymethylfurfural to diformylfuran in the presence of oxone and catalyzed by 2-iodobenzenesulfonic acid

Abstract

In the present work, an alternative system of 5-hydroxymethylfurfural (HMF) oxidation was studied, in an attempt to avoid the use of expensive metal catalysts, polluting systems and high pressures. In this context, the partial oxidation of the hydroxyl group on the HMF molecule leads to the formation of the corresponding aldehyde, 2,5-diformylfuran (DFF). This reaction was catalyzed by 2-iodobenzenesulfonic acid in the presence of oxone. Under optimized experimental conditions, the HMF conversion was found to be 100%, while the DFF yield and selectivity were almost 90%.
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Dates and versions

hal-04381898 , version 1 (09-01-2024)

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Nadim Ayoub, Carla Bergère, Joumana Toufaily, Erwann Guénin, Gérald Enderlin. A gram scale selective oxidation of 5-hydroxymethylfurfural to diformylfuran in the presence of oxone and catalyzed by 2-iodobenzenesulfonic acid. New Journal of Chemistry, 2020, 44 (27), pp.11577-11583. ⟨10.1039/D0NJ01653E⟩. ⟨hal-04381898⟩
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