Catalytic Aldol Condensation of 5‐Hydroxymethylfurfural and its Synthesis from Concentrated Feed of Carbohydrates

1‐(5‐(Hydroxymethyl)furan‐2‐yl)‐5‐methylhex‐1‐en‐3‐one was prepared from cellulose or glucose by a sequence of depolymerization/dehydration/aldol condensation reactions. The synthesis of HMF was first performed starting from a highly concentrated feed of glucose and cellulose (31 wt.%) using choline...

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Published inChemCatChem Vol. 15; no. 11
Main Authors Ramdani, Wahiba, Rabadán González, Inés, Benbakoura, Nora, Ahmar, Mohammed, Verrier, Charlie, Queneau, Yves, Pera‐Titus, Marc, Jérôme, François, De Oliveira Vigier, Karine
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 09.06.2023
Wiley
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Summary:1‐(5‐(Hydroxymethyl)furan‐2‐yl)‐5‐methylhex‐1‐en‐3‐one was prepared from cellulose or glucose by a sequence of depolymerization/dehydration/aldol condensation reactions. The synthesis of HMF was first performed starting from a highly concentrated feed of glucose and cellulose (31 wt.%) using choline chloride in MIBK/water biphasic media via the formation of a glucoside intermediate. Next, the aldol condensation of HMF with MIBK was investigated over alkaline metal oxides. Among the catalysts used, commercial BaO was highly efficient with a yield of aldol product above 90 %. Under air, BaO instantaneously transformed into Ba(OH)2, H2O and BaO2 which are regarded as active phases for the reaction. The catalyst basicity and solvent were key parameters to govern the selectivity of the reaction by limiting secondary reactions. Catalytic aldol condensation: Use of ChCl to convert a high concentrated feed of carbohydrates (glucose and ball milled cellulose) to HMF and its further conversion to 1‐(5‐(hydroxymethyl)furan‐2‐yl)‐5‐methylhex‐1‐en‐3‐one using an efficient catalyst (BaO) for the aldol condensation of HMF with ketones.
ISSN:1867-3880
1867-3899
1867-3899
DOI:10.1002/cctc.202300044