Skip to main content
Log in

In situ version of radical-chain substitution reactions

  • Organic Synthesis and Industrial Organic Chemistry
  • Published:
Russian Journal of Applied Chemistry Aims and scope Submit manuscript

Abstract

Peroxy acetals derived from an ether and a hydroperoxide can be prepared in situ and used without isolation to effect sulfochlorination of n-alkanes or chlorination of toluene to benzyl chloride.

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

References

  1. Kronman, A.R., Semchikov, Yu.D., and Kanakov, A.E., Plast. Massy, 2002, no. 8, pp. 23–30.

  2. Rakhimov, A.I., Khimiya i tekhnologiya organicheskikh perekisnykh soedinenii (Chemistry and Technology of Organic Peroxy Compounds), Moscow: Khimiya, 1979.

    Google Scholar 

  3. Kurdyukov, A.M., Izv. Vyssh. Uchebn. Zaved., Khim. Khim. Tekhnol., 2004, vol. 47, no. 1, pp. 135–140.

    CAS  Google Scholar 

  4. RF Patent 2 231 524.

  5. Weygand-Hilgetag, Organisch-chemische Experimentierkunst, Leipzig: Barth, 1964, 3rd ed.

    Google Scholar 

  6. RF Patent 2 291 144.

Download references

Author information

Authors and Affiliations

Authors

Additional information

Original Russian Text © A.M. Kurdyukov, 2007, published in Zhurnal Prikladnoi Khimii, 2007, Vol. 80, No. 9, pp. 1533–1536.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kurdyukov, A.M. In situ version of radical-chain substitution reactions. Russ J Appl Chem 80, 1566–1569 (2007). https://doi.org/10.1134/S1070427207090236

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1070427207090236

Keywords

Navigation