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Synthesis of 6-Aminobenzopentathiepines by Reactions of 4-Nitrobenzodithiol-2-ones with NaHS Full article

Journal Letters in Organic Chemistry
ISSN: 1570-1786 , E-ISSN: 1875-6255
Output data Year: 2011, Volume: 8, Number: 3, Pages: 193-197 Pages count : 5 DOI: 10.2174/157017811795038331
Tags Benzodithiol; benzopentathiepine; benzotrithiole; pentathiepine; mechanism; trithiole
Authors Khomenko Tatyana M. 1 , Korchagina Dina V. 1 , Komarova Nina I. 1 , Volcho Konstantin P. 1 , Salakhutdinov Nariman F. 1
Affiliations
1 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Lavrentiev av., 9, 630090 Novosibirsk, Russian Federation

Abstract: The reactions of benzodithiol-2-ones containing a 4-nitro group with NaHS led to mixtures of 6-aminobenzopentathiepines and 4-nitrobenzotrithiols. The product ratio and yields depend on the substituent in the aromatic ring. Based on the yields of benzopentathiepines, the following series of substituent efficiency can be inferred: CF3 >> F, Cl > CN. Aminobenzopentathiepines are probably formed via the intermediate benzotrithiols; the transformation apparently starts with the reduction of the nitro group.
Cite: Khomenko T.M. , Korchagina D.V. , Komarova N.I. , Volcho K.P. , Salakhutdinov N.F.
Synthesis of 6-Aminobenzopentathiepines by Reactions of 4-Nitrobenzodithiol-2-ones with NaHS
Letters in Organic Chemistry. 2011. V.8. N3. P.193-197. DOI: 10.2174/157017811795038331 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Mar 1, 2011
Identifiers:
Web of science: WOS:000288985000008
Scopus: 2-s2.0-79953305118
Elibrary: 16997628
OpenAlex: W2951313125
Citing:
DB Citing
Web of science 11
Scopus 12
Elibrary 11
OpenAlex 12
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