Abstract
2-perfluoroalkylperimidines were obtained by the action of trifluoroacetic anhydride and perfluoro carboxylic acid chlorides on 1,8-naphthalenediamine and its N-substituted derivatives. N,N′-Diacyl-1,8-naphthalenediamines (in the case of unsubstituted 1,8-naphthalenediamine) and 6(7)-perfluoroacyl-2-perfluoroalkylperimidines (in the case of N-substituted 1,8-naphthalenediamines) were isolated as side products.
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See [1] for communication 40.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 413–417, March, 1979.
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Pozharskii, A.F., Yurchuk, G.G. & Gervits, L.L. Heterocyclic analogs of pleiadiene. 41. synthesis of 2-perfluoroalkyl-perimidines. Chem Heterocycl Compd 15, 342–345 (1979). https://doi.org/10.1007/BF00474106
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DOI: https://doi.org/10.1007/BF00474106