Skip to main content
SpringerLink
Log in

The action of hexamethylene tetramine on phenols and the methyl esters of phenol carboxylic acids

Part IV. The synthesis and study of methyl-1-hydroxy-4-formyl 2-naphthoate and 2-acetyl-4-formyl-α-naphthol

  • Published:
Proceedings of the Indian Academy of Sciences - Section A Aims and scope Submit manuscript

Summary

Methyl-1-hydroxy-4-formyl-2-naphthoate and 2-acetyl-4-formyl-α-naphthol have been synthesised by the action of hexamethylene tetramine in glacial acetic acid, on methyl-1-hydroxy-2-naphthoate and 2-acetyl-α-naphthol respectively.

Similar formylation of 4-acetyl-α-naphthol did not succeed.

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

Access this article

Log in via an institution

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

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Desai, Radha and Shah (Under publication).

  2. Lesser, A.402, 24.

  3. Robinson and Shah, J. 1934, 1497.

Download references

Author information

Authors and Affiliations

  1. Department of Chemical Technology, University of Bombay, Bombay

    R. D. Desai, K. S. Radha & R. C. Shah

  2. Department of Chemistry, Royal Institute of Science, Bombay

    R. D. Desai, K. S. Radha & R. C. Shah

Authors
  1. R. D. Desai
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. K. S. Radha
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. R. C. Shah
    View author publications

    You can also search for this author in PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Desai, R.D., Radha, K.S. & Shah, R.C. The action of hexamethylene tetramine on phenols and the methyl esters of phenol carboxylic acids. Proc. Indian Acad. Sci. (Math. Sci.) 23, 187 (1946). https://doi.org/10.1007/BF03170936

Download citation

  • Received:

  • DOI: https://doi.org/10.1007/BF03170936

Keywords

Search

Navigation