Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/54258
Title: Significance of reagent addition sequence in the amidation of carboxylic acids mediated by PPh<inf>3</inf> and I<inf>2</inf>
Authors: Sirilak Wangngae
Chuthamat Duangkamol
Mookda Pattarawarapan
Wong Phakhodee
Keywords: Chemical Engineering
Chemistry
Issue Date: 1-Jan-2015
Abstract: © 2015 The Royal Society of Chemistry. The outcome of the amidation reaction mediated by PPh3-I2 was found to be highly dependent on the addition sequence of the reagents. When triethylamine was subjected to a mixture containing PPh3, I2, and a carboxylic acid, acid anhydride was generated almost instantly, before treatment with an amine, presumably via an attack of carboxylate ion onto the acyl function of an acyloxyphosphonium salt. Nevertheless, when a PPh3-I2 mixture was treated with an amine, then a carboxylic acid, prior to adding the base, amide was rapidly formed in high yield with high chemoselectivity, most likely through an intermediate O,N-pentacoordinate phosphorane species as confirmed by ESI-MS technique.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84943593207&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54258
ISSN: 20462069
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.