Synthesis of aldehydes from acyl chlorides via 1-(acylmethylamino)-3-methylimidazolium salts
Authors
Heras Muñoz, María Amor de lasIdentifiers
Permanent link (URI): http://hdl.handle.net/10017/2790DOI: 10.1016/0040-4039(94)02284-I
ISSN: 0040-4039
Publisher
Pergamon
Date
1995Academic Departments
Universidad de Alcalá. Departamento de Química Orgánica
Teaching unit
Unidad docente Química Orgánica
Funders
The authors are grateful for grant (MAH) from Ministerio de Educación y Ciencia
and financial support from Comisión Interministerial de Ciencia y Tecnología (CICYT) through the project
PB90-0284
Bibliographic citation
Tetrahedron Letters, 1995, v. 36, n. 3, p. 455-458
Keywords
Palladium-catalyzed reaction
Tributylin hydride
Carboxylic-acids
Reduction
Tetrahydroborate
Route
Chemistry, Organic
Project
PB90-0284 (Comisión Interministerial de Ciencia y Tecnología-CICYT)
Document type
info:eu-repo/semantics/article
Version
info:eu-repo/semantics/publishedVersion
Publisher's version
http://dx.doi.org/10.1016/0040-4039(94)02284-IRights
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Access rights
info:eu-repo/semantics/openAccess
Abstract
The reaction of acyl chlorides with 1-amino-3-methylimidazolium salts, followed by N-methylation of the resulting H-aminides, afforded 1-(acylmethylamino)-3-methylimidazolium salts which, upon treatment with DIBALHgave aldehydes in good yields. A nalogously, dialdehydes were obtained from the corresponding bis-salts.















