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Holzforschung

International Journal of the Biology, Chemistry, Physics, and Technology of Wood

Editor-in-Chief: Faix, Oskar

Editorial Board Member: Daniel, Geoffrey / Militz, Holger / Rosenau, Thomas / Salmen, Lennart / Sixta, Herbert / Vuorinen, Tapani / Argyropoulos, Dimitris S. / Balakshin, Yu / Barnett, J. R. / Berry, Richard / Burgert, Ingo / Evans, Robert / Evtuguin, Dmitry V. / Frazier, Charles E. / Fukushima, Kazuhiko / Gellerstedt, Göran / Gindl-Altmutter, Wolfgang / Glasser, W. G. / Heitner, Cyril / Holmbom, Bjarne / Isogai, Akira / Kadla, John F. / Kleen, Marjatta / Koch, Gerald / Lachenal, Dominique / Mansfield, Shawn D. / Morrell, J.J. / Niemz, Peter / Pizzi, Antonio / Ragauskas, Arthur J. / Ralph, John / Rice, Robert W. / Salin, Jarl-Gunnar / Schmitt, Uwe / Schultz, Tor P. / Schwanninger, Manfred / Sipilä, Jussi / Tamminen, Tarja / Viikari, Liisa / Welling, Johannes / Willför, Stefan / Yoshihara, Hiroshi

8 Issues per year

IMPACT FACTOR 2013: 2.339
Rank 8 out of 64 in category Forestry and 2 out of 21 in category Materials Science, Paper & Wood in the 2013 Thomson Reuters Journal Citation Report/Science Edition

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Synthesis of glucose esters from cellulose in ionic liquids

Igor A. Ignatyev1 / Charlie Van Doorslaer1 / Pascal G.N. Mertens1 / Koen Binnemans2 / 1

1Center for Surface Chemistry and Catalysis, K.U. Leuven, Heverlee, Belgium

2Department of Chemistry, Molecular Design and Synthesis, K.U. Leuven, Heverlee, Belgium

Corresponding author. Center for Surface Chemistry and Catalysis, K.U. Leuven, Kasteelpark Arenberg 23 – box 2461, B-3001, Heverlee, Belgium Phone: +32-16321610 Fax: +32-16321998

Citation Information: Holzforschung. Volume 66, Issue 4, Pages 417–425, ISSN (Online) 1437-434X, ISSN (Print) 0018-3830, DOI: 10.1515/hf.2011.161, November 2011

Publication History

Received:
2011-09-04
Accepted:
2011-10-10
Published Online:
2011-11-03

Abstract

The transformation of cellulose into glucose ester α-d-glucose pentaacetate (GPAc) was carried out in ionic liquid 1-butyl-3-methylimidazolium chloride under mild reaction conditions. The reaction comprises two steps: the first involves a hydrolysis reaction, yielding α-d-glucose and glucose oligomers; and then only after some time, the acetylating reagent acetic anhydride is added. Under optimized conditions and with the acidic resin Amberlyst 15DRY as a hydrolysis catalyst, a 70% yield of GPAc was obtained. This product could be quantitatively isolated by simple liquid-liquid extraction, which allowed easy recycling of the ionic liquid and catalyst.

Keywords: acetylation; acid catalysis; cellulose; ionic liquids; heterogeneous catalysis

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