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Synthesis of 3-fluoro-5,5,5-trinitropentanone-2 and 2-fluoro-4,4,4-trinitrobutanal

  • G. M. Nesterenko
  • L. T. Eremenko
Brief Communications Organic and Biological Chemistry
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Conclusions

  1. 1.

    Fluorination of mercury compounds with functional groups in theα-position to the mercury atom takes place at the C-Hg bond without affecting these groups.

     
  2. 2.

    The authors have obtained 2-fluoro-4,4,4-trinitrobutanal, 3-fluoro-5,5,5-trinitropentanone-2, and their 2,4-dinitrophenylhydrazones.

     

Keywords

Mercury Mercury Compound Mercury Atom 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Literature cited

  1. 1.
    L. T. Eremenko, F. Ya. Natsibullin, and G. N. Nesterenko, Izv. Akad. Nauk SSSR, Ser. Khim., 1360 (1968).Google Scholar
  2. 2.
    L. T. Eremenko and G. N. Nesterenko, Izv. Akad. Nauk SSSR, Ser. Khim., 1601 (1969).Google Scholar
  3. 3.
    Houben-Weyl, Methods of Organic Chemistry [Russian translation], Goskhimizdat (1963), p. 443.Google Scholar

Copyright information

© Consultants Bureau 1970

Authors and Affiliations

  • G. M. Nesterenko
    • 1
  • L. T. Eremenko
    • 1
  1. 1.Branch of the Institute of Chemical PhysicsAcademy of Sciences of the USSRUSSR

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