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Ultrasound-assisted one-pot synthesis of disubstituted and trisubstituted 1H-benzo[f]chromene derivatives catalyzed by 4-nitro-2,6-diacetylpyridinebis(2,4,6-trimethylaniline)FeCl2

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Abstract

1,3-Diaryl-1H-benzo[f]chromenes and 1,3-diaryl-1H-benzo[f]chromen-2-yl)(phenyl)methanones have been synthesized by one-pot three-component reaction of naphthols, aromatic aldehydes, and acetophenone or 1,3-diphenylpropane-1,3-dione, with the bis(imino)pyridine iron-based catalyst 4-nitro-2,6-diacetylpyridinebis(2,4,6-trimethylaniline)FeCl2. This novel, efficient, and rapid method is performed under solvent-free conditions with ultrasonic irradiation.

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Authors and Affiliations

  1. Department of Chemistry, Faculty of Science, University of Birjand, Birjand, Iran

    Reza Sandaroos

  2. Young Researchers Club, Sarvestan Branch, Islamic Azad University, Sarvestan, Fars, Iran

    Saman Damavandi

Authors
  1. Reza Sandaroos
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  2. Saman Damavandi
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Correspondence to Reza Sandaroos or Saman Damavandi.

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Sandaroos, R., Damavandi, S. Ultrasound-assisted one-pot synthesis of disubstituted and trisubstituted 1H-benzo[f]chromene derivatives catalyzed by 4-nitro-2,6-diacetylpyridinebis(2,4,6-trimethylaniline)FeCl2 . Res Chem Intermed 39, 4167–4174 (2013). https://doi.org/10.1007/s11164-012-0933-y

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  • DOI: https://doi.org/10.1007/s11164-012-0933-y

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