An efficient and facile synthesis of highly substituted 2,6-dicyanoanilines

J Org Chem. 2008 May 2;73(9):3596-9. doi: 10.1021/jo800260b. Epub 2008 Mar 15.

Abstract

A one-pot procedure for the synthesis of substituted 2,6-dicyanoanilines starting from readily available ynones and malononitrile has been developed. For instance, penta-1,4-diyn-3-one is converted into the acetylene-substituted aniline derivative 1 in good yield. Upon photoexcitation, this chromophore shows a strong blue emission with a high quantum yield. The ground- and the excited-state geometries, charge distributions, and excitation energies of 1 have been evaluated by ab initio calculations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aniline Compounds / chemical synthesis*
  • Aniline Compounds / chemistry
  • Crystallography, X-Ray
  • Cyanates / chemistry*
  • Malonates / chemistry
  • Models, Molecular
  • Molecular Structure
  • Spectrum Analysis

Substances

  • Aniline Compounds
  • Cyanates
  • Malonates
  • malonic acid
  • aniline