dc.contributor.author
Villorbina Noguera, Gemma
dc.contributor.author
Tomàs, Albert
dc.contributor.author
Escribà i Gelonch, Marc
dc.contributor.author
Oromí Farrús, Mireia
dc.contributor.author
Eras i Joli, Jordi
dc.contributor.author
Balcells Fluvià, Mercè
dc.contributor.author
Canela i Garayoa, Ramon
dc.date.accessioned
2024-12-05T21:25:44Z
dc.date.available
2024-12-05T21:25:44Z
dc.date.issued
2016-11-03T12:52:35Z
dc.date.issued
2025-01-01
dc.identifier
https://doi.org/10.1016/j.tetlet.2009.03.183
dc.identifier
http://hdl.handle.net/10459.1/58371
dc.identifier.uri
http://hdl.handle.net/10459.1/58371
dc.description.abstract
We describe here the first example in which glycerol has been transformed into chlorohydrin esters using an ionic liquid and hydrated aluminium chloride. The method avoids using Crown-18 ether, which was needed to obtain a similar yield when KCl was used. Alkyl and aryl acids can be used, although yields are very dependent on the carboxylic acid used.
dc.description.abstract
This work was supported by a Grant-in-Aid from the Secretaría de Estado de Política Científica y Tecnológica of the Spanish Ministry of Education and Culture (contract Grant No.: CTQ2006-07451/PPQ).
dc.relation
MIECI/PN2004-2007/CTQ2006-07451/PPQ
dc.relation
Reproducció del document publicat a https://doi.org/10.1016/j.tetlet.2009.03.183
dc.relation
Tetrahedron Letters, 2009, vol. 50, núm. 23, p. 2828–2830
dc.rights
(c) Elsevier, 2009
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.subject
Chlorohydrin esters
dc.subject
Hydrated aluminium chloride
dc.title
Combining AlCl3·6H2O and an ionic liquid to prepare chlorohydrin esters from glycerol
