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From symmetric glycerol derivatives to dissymmetric chlorohydrins
Solarte Orozco, Carmen Eugenia; Escribà i Gelonch, Marc; Eras i Joli, Jordi; Villorbina Noguera, Gemma; Canela i Garayoa, Ramon; Balcells Fluvià, Mercè
The anticipated worldwide increase in biodiesel production will result in an accumulation of glycerol for which there are insufficient conventional uses. The surplus of this by-product has increased rapidly during the last decade, prompting a search for new glycerol applications. We describe here the synthesis of dissymmetric chlorohydrin esters from symmetric 1,3-dichloro-2-propyl esters obtained from glycerol. We studied the influence of two solvents: 1,4-dioxane and 1-butanol and two bases: sodium carbonate and 1-butylimidazole, on the synthesis of dissymmetric chlorohydrin esters. In addition, we studied the influence of other bases (potassium and lithium carbonates) in the reaction using 1,4-dioxane as the solvent. The highest yield was obtained using 1,4-dioxane and sodium carbonate. This work was supported by a Grant-in-Aid from the Secretaría de Estado de Política Cientifíca y Tecnológica of the Spanish Ministry of Education and Culture (contract Grant No.: CTQ2009-14699- C02-01). The authors are grateful to the Comissionat per a Universitats i Recerca del Departament d’Innovació, Universitats i Empresa de la Generalitat de Catalunya and to the European social Fund (EFS) for the FI grant of Carmen Solarte Orozco.
-Glycerol
-Chlorohydrin esters
-Dissymmetry
-1-butanol
-Glicerina
-Èsters
cc-by, (c) Solarte et al., 2011
http://creativecommons.org/licenses/by/3.0/es/deed.ca
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Molecular Diversity Preservation International
         

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