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Esterification of Aryl/Alkyl Acids Catalysed by N-bromosuccinimide under Mild Reaction Conditions.
Cebular, Klara; Bozic, Bojan D; Stavber, Stojan.
Afiliação
  • Cebular K; Centre of Excellence for Integrated Approaches in Chemistry and Biology of Proteins, Jamova 39, 1000 Ljubljana, Slovenia. klara.cebular@ijs.si.
  • Bozic BD; Jozef Stefan International Postgraduate School, Jamova 39, 1000 Ljubljana, Slovenia. klara.cebular@ijs.si.
  • Stavber S; Department of Physical and Organic Chemistry, Jozef Stefan Institute, Jamova 39, 1000 Ljubljana, Slovenia. klara.cebular@ijs.si.
Molecules ; 23(9)2018 Sep 02.
Article em En | MEDLINE | ID: mdl-30200547
ABSTRACT
N-halosuccinimides (NXSs) are well-known to be convenient, easily manipulable and low-priced halogenation reagents in organic synthesis. In the present work, N-bromosuccinimide (NBS) has been promoted as the most efficient and selective catalyst among the NXSs in the reaction of direct esterification of aryl and alkyl carboxylic acids. Comprehensive esterification of substituted benzoic acids, mono-, di- and tri-carboxy alkyl derivatives has been performed under neat reaction conditions. The method is metal-free, air- and moisture-tolerant, allowing for a simple synthetic and isolation procedure as well as the large-scale synthesis of aromatic and alkyl esters with yields up to 100%. Protocol for the recycling of the catalyst has been proposed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bromosuccinimida / Ácidos Carboxílicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bromosuccinimida / Ácidos Carboxílicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article