Isoimides of benzene-1,2-dicarboxylic acid and napthalene-1,8-dicarboxylic acid. Suitable conditions for preparation

Authors

  • Э. B. Ганин Physicochemical Institute for the Protection of Man and the Environment, Ministry of Education and Academy of Sciences of Ukraine, Odessa 270100

Abstract

N-Arylisophthalimides are formed in an aprotic solvent at 20°C from equivalent quantities of phthaloyl chloride and an arylamine in the presence of not less than 1 mole of a dehydrochlorinating reagent. N-Nitrophenylisonaphthalimides were obtained by the reaction of an equimolar mixture of naphthaloyl chloride and nitroanilines in boiling toluene.

How to Cite
Ganin, E. V. Chem. Heterocycl. Compd. 1997, 33, 1092. [Khim. Geterotsikl. Soedin. 1997, 1251.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02253225

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Published

1997-09-25

Issue

No. 9 (1997)

Section

Original Papers