2017
DOI: 10.1016/j.cattod.2016.12.019
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Insights into the metal salt catalyzed ethyl levulinate synthesis from biorenewable feedstocks

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Cited by 34 publications
(19 citation statements)
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“…124 Acid catalysis, mainly by Brønsted acids, is also required to transform 5-hydroxymethylfurfural into levulinic acid and its esters. While levulinic acid is produced by direct hydration of HMF under acid conditions, Quereshi's group 125 proposed a mechanism for the synthesis of alkyl levulinates based on two reaction pathways (Fig. 5): hydration of HMF to LA, which is esterified to its ester depending on the alcohol used for the alcoholysis, and/or HMF is converted to alkyl levulinates via HMF-ether intermediate, as via 5-ethoxymethylfurfural (EMF) for ethyl levulinate production 126 or 5butoxymethylfurfural (BMF) for butyl levulinate.…”
Section: Production From Precursors: 5-hmf Furfural and Derivatesmentioning
confidence: 99%
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“…124 Acid catalysis, mainly by Brønsted acids, is also required to transform 5-hydroxymethylfurfural into levulinic acid and its esters. While levulinic acid is produced by direct hydration of HMF under acid conditions, Quereshi's group 125 proposed a mechanism for the synthesis of alkyl levulinates based on two reaction pathways (Fig. 5): hydration of HMF to LA, which is esterified to its ester depending on the alcohol used for the alcoholysis, and/or HMF is converted to alkyl levulinates via HMF-ether intermediate, as via 5-ethoxymethylfurfural (EMF) for ethyl levulinate production 126 or 5butoxymethylfurfural (BMF) for butyl levulinate.…”
Section: Production From Precursors: 5-hmf Furfural and Derivatesmentioning
confidence: 99%
“…5): hydration of HMF to LA, which is esterified to its ester depending on the alcohol used for the alcoholysis, and/or HMF is converted to alkyl levulinates via HMF-ether intermediate, as via 5-ethoxymethylfurfural (EMF) for ethyl levulinate production 126 or 5butoxymethylfurfural (BMF) for butyl levulinate. 127 Limited water content in the reacting mixture leads to favoring the second route in which 5-alcoxymethylfurfurals are major intermediates 125 instead of hydration to levulinic acid. Also in this case, a dedicated sustainability assessment should be carried out to quantify the comparison among the routes.…”
Section: Production From Precursors: 5-hmf Furfural and Derivatesmentioning
confidence: 99%
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“…Quereshi et al studied the production of EL from 5-hydroxymethylfuran using CuCl 2 and FeCl 3 as catalysts and obtained the EL yields of 47.5% and 43.3%, respectively. 101 Ionic liquids can replace the traditonal organic solvents and electrolytes as the medium of chemical reaction and electrochemical system. Its unique adjustable electrostic field, special ionic envrionment and multi-dimensional weak interaction make it easy to adopt effective means to regulate the catalytic activity and selectivity.…”
Section: Levulinate Estersmentioning
confidence: 99%
“…Quereshi et al . studied the production of EL from 5‐hydroxymethylfuran using CuCl2 and FeCl3 as catalysts and obtained the EL yields of 47.5% and 43.3%, respectively 101 . Ionic liquids can replace the traditonal organic solvents and electrolytes as the medium of chemical reaction and electrochemical system.…”
Section: Transformation Of La To Valuable Chemicalsmentioning
confidence: 99%