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Reactions of 4-substituted-1-[(difluoromethyl)sulfinyl]polyfluorobenzenes with phenolate anion Full article

Journal ARKIVOC
ISSN: 1551-7004 , E-ISSN: 1551-7012
Output data Year: 2020, Pages: 344-361 Pages count : 18 DOI: 10.24820/ark.5550190.p011.262
Tags Polyfluoroaromatic compounds; sulfoxides; sodium phenolate; aromatic nucleophilic substitution
Authors Koshcheev Borislav V. 1 , Bredikhin Roman A. 1 , Maksimov Alexander M. 1 , Platonov Vyacheslav E. 1 , Andreev Rodion V. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: The reactions of 4-substituted-polyfluorinated-[(difluoromethyl)sulfinyl]benzenes ([4-X-C6F4S(O)CHF2 [X = H, CF3 and C6F5S(O)]) with phenolate anion in benzene, Et2O and CH3CN have been investigated. The reactions of the substrate (X = H, CF3) and sodium phenolate in equal amounts resulted in the formation of mixtures of the starting compound, 2-phenoxyderivative and disubstituted products. The two-fold amount of the phenolate afforded the 2,6-disubstituted products for X = H in MeCN and for X = CF3 in Et2O. At the same time, 4-CF3-C6F4S(O)CHF2 in CH3CN gave a mixture of the 2,6- and 2,5-bis(phenoxy) derivatives. Quantum chemical calculations have been performed to explain this phenomenon. For X = C 6 F 5 S(0) in MeCN, the reaction was accompanied by sulfinyl moiety ipso-substitution. [GRAPHICS] .
Cite: Koshcheev B.V. , Bredikhin R.A. , Maksimov A.M. , Platonov V.E. , Andreev R.V.
Reactions of 4-substituted-1-[(difluoromethyl)sulfinyl]polyfluorobenzenes with phenolate anion
ARKIVOC. 2020. P.344-361. DOI: 10.24820/ark.5550190.p011.262 WOS Scopus OpenAlex
Files: Full text from publisher
Dates:
Published online: Sep 21, 2020
Identifiers:
Web of science: WOS:000584517600030
Scopus: 2-s2.0-85094142769
OpenAlex: W3088526293
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