Skip to main content
Log in

Summary

  1. 1.

    N-Piperidinocarbinol has been prepared for the first time.

  2. 2.

    N-Piperidinocarbinol is converted spontaneously into N,N'-bis-piperidinomethane, condenses easily with methanol, amines, and 2-nitropropane, but does not react with phenylacetylene.

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.

Literature cited

  1. L. Henry, Bull. Soc. chim. France13, 157 (1895).

    Google Scholar 

  2. N. Putokhin, ZhRFKho,59, 804 (1927).

    Google Scholar 

  3. H. Hellman and G. Opitz, Ber.89, 81 (1956).

    Google Scholar 

  4. H. G. Jonson, J. Amer. Chem. Soc.68, 14 (1946).

    Google Scholar 

  5. R. G. Kostyanovskii and V. F. Bystrov, Izv. AN SSSR, Otd. khim. n.,1962, 1488.

  6. E. C. Wagner, J. Organ. chem.19, 1862 (1954).

    Google Scholar 

  7. C. Mannich and F. Chang, Ber.66, 418 (1933).

    Google Scholar 

  8. H. Böhme et al., Ber.91, 340 (1958);92, 2976 (1959).

    Google Scholar 

  9. R. G. Kostyanovskii, O. A. Pan'shin, and V. F. Bystrov, Izv. AN SSSR, Otd. khim. n.,1962, No. 5, 931.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kostyanovskii, P.G., Pan'shin, O.A. N-piperidinocarbinol. Russ Chem Bull 12, 164–167 (1963). https://doi.org/10.1007/BF00846972

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00846972

Keywords

Navigation