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Benzindoles. 21. Nitration of 3-formyl[4, 5]-and 3-formyl [6,7] benzindoles
Authors:O. D. Zhilina  L. B. Shagalov  A. M. Vasil'ev  N. N. Suvorov
Affiliation:(1) Institute of Biophysics, Ministry of Public Health of the USSR, 123182 Moscow;(2) D. I. Mendeleev Moscow Institute of Chemical Technology, 125047 Moscow
Abstract:It was established that products of monosubstitution of 4-nitro- and 7-nitro-3-formyl[4,5] benzindoles and products of disubstitution of 4,8-dinitro- and 7,8-dinitro-3-formyl [4,5] benzindoles are formed in low yields in the nitration of 3-formyl [4,5]benzindole with sodium nitrate in concentrated sulfuric acid. Similar nitration of 3-formyl [6,7] benzindole leads to 9-nitro- and 5, 6-dinitro-3-formyl [6,7]benzindoles. The 3-formylnitrobenzindoles obtained were converted to nitrovinyl derivatives by condensation with nitromethane.See [1] for Communication [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 949–955, July, 1980.
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