Divinyl ethers of glycols in homolytic reactions with carbon tetrachloride and aldehydes

  • A. S. Atavin
  • G. M. Gavrilova
  • B. A. Trofimov
Organic and Biological Chemistry


  1. 1.

    The bis-(1,3,3-trichloroallyl) ether of ethylene glycol was isolated as the result of the homolytic addition of carbon tetrachloride to the divinyl ethers of diols.

  2. 2.

    The homolytic reaction of aldehydes with the divinyl ethers of diols leads to a complex mixture of products, the greater part of which apparently represent oligomers.



Ether Glycol Aldehyde Oligomer Diol 
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.


Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    E. Levas, Compt. Rend.,230, 1669 (1950).Google Scholar
  2. 2.
    E. Levas and M. Levas, Compt. Rend.,232, 521 (1951).Google Scholar
  3. 3.
    M. Levas, Ann. Chim. (Paris),7, 697 (1952).Google Scholar
  4. 4.
    A. Glickman, US Patent No. 2560219; Chem. Abstrs.,46, 1023 (1952).Google Scholar
  5. 5.
    Kh. S. Bagdasar'yan and R. I. Milyutinskaya, Zh. Fiz. Khim.,28, 498 (1954).Google Scholar
  6. 6.
    A. F. Revzin and Kh. S. Bagdasar'yan, Zh. Fiz. Khim.,38, 215 (1964).Google Scholar
  7. 7.
    M. F. Shostakovskii, A. V. Bogdanova, M. M. Zverov, and G. I. Plotnikova, Izv. Akad. Nauk SSSR, Otd. Khim. Nauk, 1236 (1956).Google Scholar
  8. 8.
    A. V. Bogdanova and M. F. Shostakovskii, Izv. Akad. Nauk SSSR, Otd. Khim. Nauk, 224 (1957).Google Scholar
  9. 9.
    M. Levas and E. Levas, Compt. Rend.,246, 2630 (1958).Google Scholar
  10. 10.
    M. Levas and E. Levas, Bull. Soc. Chim. France, 1598 (1965).Google Scholar
  11. 11.
    A. V. Bogdanova, M. F. Shostakovskii, and G. K. Krasil'nikova, Izv. Akad. Nauk SSSR, Otd. Khim., Nauk, 345 (1957).Google Scholar
  12. 12.
    M. F. Shostakovskii, A. V. Bogdanova, G. I. Plotnikova, and E. V. Dubrova, Izv. Akad. Nauk SSSR, Otd. Khim. Nauk, 756 (1958).Google Scholar
  13. 13.
    S. N. Ushakov, S. P. Mitsengendler, and V. N. Krasulina, Izv. Akad. Nauk SSSR, Otd. Khim. Nauk, 366 (1957).Google Scholar
  14. 14.
    F. M. Lewis and F. R. Mayo, J. Amer. Chem. Soc.,76, 457 (1954).Google Scholar
  15. 15.
    C. Walling and E. S. Huyser, in: Organic Reactions [Russian translation], Vol. 13, Mir (1966), p. 110.Google Scholar
  16. 16.
    G. I. Nikishin, M. G. Vinogradov, and R. V. Kereselidze, Zh. Organ. Khim.,2, 1918 (1966).Google Scholar
  17. 17.
    Youichi Sasajima, Kensuke Shima, and Hiroshi Sakurai, Nippon Kagaku Zasshi,86, 1299, A76 (1965); Ref. Khim. Zh., 16zh, 178 (1967); Chem. Abstrs.,65, 13491d (1966).Google Scholar
  18. 18.
    B. A. Trofimov, A. S. Atavin, G. M. Gavrilova, and G. A. Kalabin, Zh. Obshch. Khim.,38, 2344 (1968).Google Scholar

Copyright information

© Consultants Bureau 1972

Authors and Affiliations

  • A. S. Atavin
    • 1
  • G. M. Gavrilova
    • 1
  • B. A. Trofimov
    • 1
  1. 1.Irkutsk Institute of Organic ChemistrySiberian Branch of the Academy of Sciences of the USSRUSSR

Personalised recommendations