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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2000 Volume 10, Issue 2, Pages 78–80 (Mi mendc4393)

This article is cited in 18 papers

The differing reactivity of the bromo and nitro groups in 4-bromo-5-nitrophthalonitrile towards nucleophilic attack

I. G. Abramov, M. V. Dorogov, S. A. Ivanovskii, A. V. Smirnov, M. B. Abramova

Department of Organic Chemistry, Yaroslavl State Technical University, Yaroslavl, Russian Federation

Abstract: The high reactivity of 4-bromo-5-nitrophthalonitrile and different mobilities of the leaving groups (bromo and nitro) in aromatic nucleophilic substitution reactions offer new opportunities for the synthesis of substituted phthalonitriles and then various heterocyclic compounds.

Language: English

DOI: 10.1070/MC2000v010n02ABEH001147



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