A new method for N-N bond cleavage of N,N-disubstituted hydrazines to secondary amines and direct ortho amination of naphthol and its analogues

J Am Chem Soc. 2008 May 7;130(18):5840-1. doi: 10.1021/ja711153b. Epub 2008 Apr 12.

Abstract

An unexpected reaction of N,N-disubstituted hydrazine with naphthol and its analogues under simply thermal conditions has been disclosed. 2-Naphthol reacted with various N,N-disubstituted hydrazines under argon to afford 1-amino-2-naphthol and the corresponding secondary amines in excellent yields. Ortho amination of 2-naphthols, hydroxyquinoline, and naphthalenamine occurred when they reacted with N-methyl-N-phenylhydrazine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amination
  • Amines / chemical synthesis*
  • Hydrazines / chemistry*
  • Hydroxyquinolines / chemistry
  • Naphthalenes / chemistry
  • Naphthols / chemical synthesis
  • Naphthols / chemistry*
  • Phenylhydrazines / chemistry

Substances

  • Amines
  • Hydrazines
  • Hydroxyquinolines
  • Naphthalenes
  • Naphthols
  • Phenylhydrazines
  • 4-methylphenylhydrazine