Skip to main content
Log in

Cyclic unsaturated compounds

Communication 29. Pentamethylcyclopentadienes

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

Conclusions

  1. 1.

    The methylation of sodium 1,2,3,4-tetramethylcyclopentadienyl in liquid ammonia gives a mixture that analyzes 88% of 1,2,4,5,5-pentamethylcyclopentadiene and 12% of 1,2,3,4,5-pentamethylcyclopentadiene. The methylation of the latter leads to the formation of hexamethylcyclopentadiene in good yield.

  2. 2.

    We were the first to discover the 1,3-migration of a methyl group in the cyclopentadiene ring. At 425–500°, 1,2,4,5,5-pentamethylcyclopentadiene is smoothly isomerized to 1,2,3,4,5-pentamethylcyclopentadiene. The coupling of two consecutive intramolecular acts of 1,2-migration of the methyl group is considered to be the mechanism of such isomerization. The pyrolysis of the readily available 1,2,4,5,5-pentamethylcyclopentadiene is a convenient preparative method for the synthesis of 1,2,3,4,5-pentamethylcyclopentadiene.

  3. 3.

    The obtained dienes were characterized by the adducts with maleic anhydride and their derivatives. A study was made of the stereochemistry of the condensation products of 1,2,3,4,5-pentamethylcyclopentadiene with maleic anhydride. The 7-syn isomer (with respect to the double bond) predominates in the mixture of epimers formed at the C7 center of the bicyclo[2.2.1]heptene system.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature cited

  1. V. A. Mironov, T. M. Fadeeva, V. S. Pashegorova, A. U. Stepanyants, and A. A. Akhrem. Izv. Akad. Nauk SSSR, Ser. Khim.,1968, 423.

  2. L. deVries, J. Org. Chem.,25, 1838 (1960).

    Google Scholar 

  3. V. A. Mironov, T. M. Fadeeva, E. V. Sobolev, and A. N. Elizarova, Zh. Obshch. Khim.,33, 84 (1963).

    Google Scholar 

  4. V. A. Mironov, E. V. Sobolev, and A. N. Elizarova, Tetrahedron,19, 1939 (1963).

    Google Scholar 

  5. R. Ya. Levina, N. N. Mezentseva, and E. G. Treshcheva, Dokl. Akad. Nauk SSSR,104, 549 (1955).

    Google Scholar 

  6. R. Riemschneider and E. B. Grabitz, Monatsh. Chem.,89, 748 (1958).

    Google Scholar 

  7. S. McLean and P. Haynes, Tetrahedron,21, 2343 (1965).

    Google Scholar 

  8. V. A. Mironov, E. V. Sobolev, and A. N. Elizarova, Izv. Akad. Nauk SSSR, Ser. Khim.,1964, 1607.

  9. V. A. Mironov, S. N. Kostina, E. V. Sobolev, and A. N. Elizarova, Izv. Akad. Nauk SSSR, Ser. Khim.,1964, 864.

  10. V. A. Mironov, S. N. Kostina, and A. N. Elizarova, Izv. Akad. Nauk SSSR, Ser. Khim.,1964, 875.

  11. K. Alder and R. Muders, Chem. Ber.,91, 1083 (1958).

    Google Scholar 

  12. B. F. Hallam and P. L. Pauson, J. Chem. Soc,1958, 646.

  13. B. A. Kazanskii, E. V. Sobolev, V. T. Aleksanyan, L. A. Nakhapetyan, and M. Yu. Lukina, Dokl. Akad. Nauk SSSR,159, 839 (1964).

    Google Scholar 

  14. J. W. de Haan and H. Kloosterziel, Rec. Trav. Chim.,84, 1594 (1965).

    Google Scholar 

  15. V. A. Mironov, T. M. Fadeeva, and A. A. Akhrem, Dokl. Akad. Nauk SSSR,174, 852 (1967).

    Google Scholar 

  16. V.F. Bystrov, A. U. Stepanyants, and V. A. Mironov, Zh. Obshch. Khim.,34, 2886 (1964).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

See [1] for Communication 28 in the given series.

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 609–621, March, 1968.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mironov, V.A., Pashegorova, V.S., Fadeeva, T.M. et al. Cyclic unsaturated compounds. Russ Chem Bull 17, 588–597 (1968). https://doi.org/10.1007/BF00911617

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00911617

Keywords

Navigation