A rapid mild esterification method
- 1 January 1972
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 2 (4), 215-219
- https://doi.org/10.1080/00397917208081770
Abstract
The well known method for the formation of carboxylate esters by the reactions of alkyl halides with metal salts of Carboxylates (where M includes Ag, pb, and alkali metals) is not a generally useful synthetic method1. Several improvements have increased the utility of this method2–5.Chief among them is the use of ammonium salts rather than metal salts. Moreover, amines and quaternary ammonium salts in catalytic amouts also increase the rate of the reactions, i.e., at room temparature or below except when highly active alkyl halides are employed.Keywords
This publication has 4 references indexed in Scilit:
- Direct Esterification of Carboxylic Acid with Alkyl Halide by Cu(I) OxideSynthetic Communications, 1972
- Beitrag zur katalytischen Veresterung von Carbonsäuresalzen mit AlkylhalogenidenJournal für Praktische Chemie, 1971
- Exploratory Process Study. Base-Catalyzed Reaction of Organic Chlorides with Sodium AcetateProduct R&D, 1969
- Esters from the Reactions of Alkyl Halides and Salts of Carboxylic Acids. Comprehensive Study of Amine CatalysisI&EC Product Research and Development, 1968