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Nitration of N-Chloromethyl-substituted secondary amides by nitronium tetrafluoborate

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

When treated with nitronium tetrafluoborate the N-chloromethyi derivatives of the secondary amides of the carbonic, sulfonic, and nitric acids form either the corresponding N-alkyl-N-nitramides, methylenebis-N-alkylamides, or their mixture.

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Literature cited

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Authors and Affiliations

  1. N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow

    O. A. Luk'yanov, T. G. Mel'nikova, E. G. Kashirskaya & V. A. Tartakovskii

Authors
  1. O. A. Luk'yanov
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  2. T. G. Mel'nikova
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  3. E. G. Kashirskaya
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  4. V. A. Tartakovskii
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1182–1184, May, 1982.

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Luk'yanov, O.A., Mel'nikova, T.G., Kashirskaya, E.G. et al. Nitration of N-Chloromethyl-substituted secondary amides by nitronium tetrafluoborate. Russ Chem Bull 31, 1055–1057 (1982). https://doi.org/10.1007/BF00949972

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  • DOI: https://doi.org/10.1007/BF00949972

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