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Synthesis of benzotristriazole. 4-nitrobenzo[1,2-d:3,4-d′] bistriazole and 4,4′-dicarboxy-5,5′-1H-1,2,3-triazole Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 1993, Volume: 29, Number: 10, Pages: 1169-1171 Pages count : 3 DOI: 10.1007/BF00538063
Authors Samsonov V.A. 1 , Volodarskii L.B. 1 , Korolev V.L. 1 , Khisamutdinov G.Kh. 1
Affiliations
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation

Abstract: The treatment of 2,5,8-tri(2,4-dinitrophenyl)benzotristriazole, 2,7-di(2,4-dinitrophenyl)-4-nitrobenzo[1,2-d:3,4-d′]bistriazole, and 4,4′-dicarboxy-5,5′-bis[2- (2,4-dinitrophenyl)-2H-1,2,3-triazole with sodium methylate leads to loss of the 2,4-dinitrophenyl group as 2,4-dinitroanisole and formation of benzotristriazole, 4-nitrobenzo[1,2-d:3,4-d′]bistriazole, and 4,4′-dicarboxy-5,5′-bis-1H-1,2,3-triazole, respectively, in good yields. © 1994 Plenum Publishing Corporation.
Cite: Samsonov V.A. , Volodarskii L.B. , Korolev V.L. , Khisamutdinov G.K.
Synthesis of benzotristriazole. 4-nitrobenzo[1,2-d:3,4-d′] bistriazole and 4,4′-dicarboxy-5,5′-1H-1,2,3-triazole
Chemistry of Heterocyclic Compounds. 1993. V.29. N10. P.1169-1171. DOI: 10.1007/BF00538063 Scopus РИНЦ OpenAlex
Dates:
Published print: Oct 1, 1993
Identifiers:
Scopus: 2-s2.0-11544252042
Elibrary: 31099956
OpenAlex: W2088503875
Citing:
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Scopus 5
Elibrary 4
OpenAlex 2
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