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Reactions of polyfluoroaromatic compounds with electrophilic agents in the presence of tris(dialkylamino) phosphines .8. Replacement of fluorine by hydrogen in polyfluoroaromatic compounds Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 1997, Volume: 46, Number: 8, Pages: 1434-1436 Pages count : 3 DOI: 10.1007/BF02505680
Tags polyfluoroarenes; reduction; tris(diethylamino)phosphine
Authors Bardin V.V. 1
Affiliations
1 Novosibirsk Institute of Organic chemistry, Novosibirsk 630090, Russia

Abstract: When reacted with P(NEt2)(3) and a proton donor, pentafluoropyridine, 3-chlorotetrafluoropyridine, pentafluorobenzonitrile, and octafluorotoluene yield products of replacement of the fluorine atom by hydrogen at position 4. This process is accompanied by the side reaction of aminodefluorination. In the case of 3-H-heptafluorotoluene and octafluoronaphthalene, aminodefluorination is the main reaction. Reactions of perfluoro-4-isopropyltoluene, 4-H-heptafluorotoluene, and 4-methylheptafluorotoluene do not occur under the above-mentioned conditions.
Cite: Bardin V.V.
Reactions of polyfluoroaromatic compounds with electrophilic agents in the presence of tris(dialkylamino) phosphines .8. Replacement of fluorine by hydrogen in polyfluoroaromatic compounds
Russian Chemical Bulletin. 1997. V.46. N8. P.1434-1436. DOI: 10.1007/BF02505680 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Aug 1, 1997
Identifiers:
Web of science: WOS:A1997YE52900013
Scopus: 2-s2.0-0031495908
Elibrary: 13269433
OpenAlex: W2335349394
Citing:
DB Citing
Web of science 2
Scopus 1
Elibrary 1
OpenAlex 2
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