A two-step approach for the catalytic conversion of glucose to 2,5-dimethylfuran in ionic liquids
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- 28 May 2010
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 12 (7), 1253-1262
- https://doi.org/10.1039/c004343e
Abstract
Lignocellulosic biomass is an attractive resource for producing transportation fuels, and consequently novel approaches are being sought for transforming the lignin and cellulosic constituents of biomass to fuels or fuel additives. Glucose, the monomer of cellulose, is a good starting material for exploring such chemistries. We report here the results of an investigation aimed at identifying catalysts for the dehydration of glucose to 5-hydroxymethylfurfural (HMF) dissolved in ionic liquids and the subsequent conversion of HMF to 2,5-dimethylfuran (DMF), a high-energy content product that could be used as a fuel or fuel additive. Heteropoly acids were found to be exceptionally active and selective catalysts for the dehydration of glucose. Nearly 100% yield of HMF could be achieved using 12-molybdophosphoric acid (12-MPA) in a solution of 1-ethyl-3-methylimidazolium chloride (EMIMCl) and acetonitrile. The addition of acetonitrile to EMIMCl suppressed the formation of humins from glucose. The high HMF selectivity achievable with heteropoly acid catalysts is ascribed to stabilization of 1,2-enediol and other intermediates involved in the dehydration of glucose and the avoidance of forming the 2,3-enediol intermediate leading to furylhydroxymethyl ketone (FHMK). Carbon-supported metals, and in particular Pd/C, were effective in promoting the hydrogenation of HMF dissolved in EMIMCl and acetonitrile to DMF. The following intermediates were observed in the hydrogenation of HMF to DMF: 5-methylfurfural (MF), 5-methylfurfyl alcohol (MFA), and 2,5-dihydroxymethylfuran (DHMF). The relative rate of formation and consumption of these compounds was explored by using each of them as a reactant in order to identify the reaction pathway from HMF to DMF. It was also observed that HMF produced via glucose dehydration could be converted to DMF without isolation, if the dehydration catalyst, 12 MPA, was replaced by the hydrogenation catalyst, Pd/C. This two-step catalytic approach provides the basis for completely converting glucose to HMF and further converting HMF to DMF.Keywords
This publication has 47 references indexed in Scilit:
- Ionic Liquids and Their Interaction with CelluloseChemical Reviews, 2009
- High-throughput screening for ionic liquids dissolving (ligno-)celluloseBioresource Technology, 2009
- Dissolution of Wood in Ionic LiquidsJournal of Agricultural and Food Chemistry, 2007
- Applications of Ionic Liquids in Carbohydrate Chemistry: A Window of OpportunitiesBiomacromolecules, 2007
- One-Step Conversion of Cellobiose to C6-Alcohols Using a Ruthenium Nanocluster CatalystJournal of the American Chemical Society, 2006
- Dissolution of cellulose with ionic liquids and its application: a mini-reviewGreen Chemistry, 2006
- Room-temperature ionic liquids that dissolve carbohydrates in high concentrationsGreen Chemistry, 2004
- Characterizing Ionic Liquids On the Basis of Multiple Solvation InteractionsJournal of the American Chemical Society, 2002
- Unsaturated O- and N-Heterocycles from Carbohydrate FeedstocksAccounts of Chemical Research, 2002
- Dissolution of Cellose with Ionic LiquidsJournal of the American Chemical Society, 2002