Significance of reagent addition sequence in the amidation of carboxylic acids mediated by PPh<inf>3</inf> and I<inf>2</inf>

• Main Authors: Sirilak Wangngae, Chuthamat Duangkamol, Mookda Pattarawarapan, Wong Phakhodee
• Format: Journal
• Published: 2018
• Subjects: Chemical Engineering; Chemistry
• Online Access: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84943593207&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/54258
• Institution: Chiang Mai University

© 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.