Skip to main content
Log in

Chemical polarization of nuclei

5. Interaction of 2,6-di-tert-butyl-1,4-benzoquinonediazide with primary aliphatic amines

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

Conclusions

The reaction of 2,6-di-tert-butyl-1,4-benzoquinonediazide with primary aliphatic amines leads to the formation of intermediate unstable triazenes which, in turn, break down through a radical mechanism to form 2,6-di-tert-butylphenol and 2,6-di-tert-butyl-p-benzoquinone, the final reaction products.

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. Sh. A. Markaryan, L. G. Plekhanova, G. A. Nikiforov, S. V. Rykov, V. V. Ershov and A. L. Buchachenko, Izv. Akad. Nauk SSSR, Ser. Khim., 2620 (1972).

  2. G. A. Nikiforov, A. A. Efremenko and V. V. Ershov, Izv. Akad. Nauk SSSR, Ser. Khim., 2702 (1967).

  3. G. A. Nikoforov, L. G. Plekhanova, A. A. Efremenko, D. G. Pobedimskii and V. V. Ershov, Izv. Akad. Nauk SSSR, Ser. Khim., 146 (1971).

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 771–775, April, 1977.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nikiforov, G.A., Pershin, A.D., Kende, I. et al. Chemical polarization of nuclei. Russ Chem Bull 26, 700–704 (1977). https://doi.org/10.1007/BF01108184

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01108184

Keywords

Navigation