One-Pot Synthesis of Levulinic Acid/Ester from C5 Carbohydrates in a Methanol Medium

A process for direct conversion of xylose to methyl levulinate and levulinic acid has been developed in this study. A methanol medium, solid acid catalyst Amberlyst 70, and hydrogenation catalyst Pd/Al2O3 were used to direct xylose to follow the designed route to the target products. The methanol me...

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Main Authors: Hu, Xun, Song, Yao, Wu, Liping, Gholizadeh, Mortaza, Li, Chun-Zhu
Format: Journal Article
Published: American Chemical Society 2013
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/42618
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author Hu, Xun
Song, Yao
Wu, Liping
Gholizadeh, Mortaza
Li, Chun-Zhu
author_facet Hu, Xun
Song, Yao
Wu, Liping
Gholizadeh, Mortaza
Li, Chun-Zhu
author_sort Hu, Xun
building Curtin Institutional Repository
collection Online Access
description A process for direct conversion of xylose to methyl levulinate and levulinic acid has been developed in this study. A methanol medium, solid acid catalyst Amberlyst 70, and hydrogenation catalyst Pd/Al2O3 were used to direct xylose to follow the designed route to the target products. The methanol medium can prevent the hydrogenation of xylose to xylitol via the transformation of xylose into methyl xylosides. Amberlyst 70 catalyzes the dehydration of methyl xylosides into furfural, while Pd/Al2O3 catalyzes the hydrogenation of furfural into furfuryl alcohol. The hydrolysis/methanolysis of furfuryl alcohol over Amberlyst 70 produces levulinic acid/ester. Among these steps, the hydrogenation of furfural is the one determining the overall selectivity from xylose to levulinic acid/ester. The ideal hydrogenation catalyst needs to be selective to hydrogenate only the carbonyl group of furfural but not the furan rings.
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institution Curtin University Malaysia
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publishDate 2013
publisher American Chemical Society
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spelling curtin-20.500.11937-426182017-09-13T14:24:48Z One-Pot Synthesis of Levulinic Acid/Ester from C5 Carbohydrates in a Methanol Medium Hu, Xun Song, Yao Wu, Liping Gholizadeh, Mortaza Li, Chun-Zhu C5 carbohydrates acid-catalyzed conversion furfural levulinic acid hydrogenation A process for direct conversion of xylose to methyl levulinate and levulinic acid has been developed in this study. A methanol medium, solid acid catalyst Amberlyst 70, and hydrogenation catalyst Pd/Al2O3 were used to direct xylose to follow the designed route to the target products. The methanol medium can prevent the hydrogenation of xylose to xylitol via the transformation of xylose into methyl xylosides. Amberlyst 70 catalyzes the dehydration of methyl xylosides into furfural, while Pd/Al2O3 catalyzes the hydrogenation of furfural into furfuryl alcohol. The hydrolysis/methanolysis of furfuryl alcohol over Amberlyst 70 produces levulinic acid/ester. Among these steps, the hydrogenation of furfural is the one determining the overall selectivity from xylose to levulinic acid/ester. The ideal hydrogenation catalyst needs to be selective to hydrogenate only the carbonyl group of furfural but not the furan rings. 2013 Journal Article http://hdl.handle.net/20.500.11937/42618 10.1021/sc400229w American Chemical Society restricted
spellingShingle C5 carbohydrates
acid-catalyzed conversion
furfural
levulinic acid
hydrogenation
Hu, Xun
Song, Yao
Wu, Liping
Gholizadeh, Mortaza
Li, Chun-Zhu
One-Pot Synthesis of Levulinic Acid/Ester from C5 Carbohydrates in a Methanol Medium
title One-Pot Synthesis of Levulinic Acid/Ester from C5 Carbohydrates in a Methanol Medium
title_full One-Pot Synthesis of Levulinic Acid/Ester from C5 Carbohydrates in a Methanol Medium
title_fullStr One-Pot Synthesis of Levulinic Acid/Ester from C5 Carbohydrates in a Methanol Medium
title_full_unstemmed One-Pot Synthesis of Levulinic Acid/Ester from C5 Carbohydrates in a Methanol Medium
title_short One-Pot Synthesis of Levulinic Acid/Ester from C5 Carbohydrates in a Methanol Medium
title_sort one-pot synthesis of levulinic acid/ester from c5 carbohydrates in a methanol medium
topic C5 carbohydrates
acid-catalyzed conversion
furfural
levulinic acid
hydrogenation
url http://hdl.handle.net/20.500.11937/42618