Abstract
N-Pentafluorophenylcarbonimidoyl dichloride reacts with aromatic hydrocarbons (benzene, toluene, xylenes, and mesitylene) in the presence of AlCl3 to give stableN-pentafluorophenylbenzimidoyl chlorides, which can further react with aromatic hydrocarbons to give azomethine derivatives. An increase in the number of methyl groups in the molecule of a hydrocarbon favors the reaction.
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Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1605–1611, September, 1993.
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Petrova, T.D., Kolesnikova, I.V., Mamatyuk, V.I. et al. Reactions ofN-pentafluorophenylcarbonimidoyl dichloride with aromatic hydrocarbons in the presence of aluminum chloride. Russ Chem Bull 42, 1540–1546 (1993). https://doi.org/10.1007/BF00699191
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DOI: https://doi.org/10.1007/BF00699191