Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/65485
Title: Metal-Free Synthesis of 2-N,N-Dialkylaminobenzoxazoles Using Tertiary Amines as the Nitrogen Source
Authors: Mookda Pattarawarapan
Dolnapa Yamano
Nitaya Wiriya
Wong Phakhodee
Keywords: Chemistry
Issue Date: 17-May-2019
Abstract: © 2019 American Chemical Society. The unprecedented reaction of tertiary amines with 2(3H)-benzoxazolones has been investigated. In the presence of the Ph 3 P-I 2 reagent system, the reaction of both acyclic and cyclic aliphatic tertiary amines led to the formation of 2-N,N-dialkylaminobenzoxazoles with the selective cleavage of an alkyl group. Especially, N-(2-iodoethyl)piperazinyl derivatives were rapidly produced in good yields when using DABCO as the nitrogen source. Only in the cases when the nucleophilicity of the substrates exceeds that of the amine, competitive self-condensation of benzoxazolones then proceeds preferentially. 31 P{ 1 H}-NMR study suggested the involvement of an aryloxyphosphonium intermediate and/or possibly 2-iodobenzoxazole which activates the C-2 position of benzoxazolones toward nucleophilic aromatic substitution.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85065768637&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/65485
ISSN: 15206904
00223263
Appears in Collections:CMUL: Journal Articles

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