4.5 Article

Green and efficient synthesis of acridine-1,8-diones and hexahydroquinolines via a KH2PO4 catalyzed Hantzsch-type reaction in aqueous ethanol

Journal

RESEARCH ON CHEMICAL INTERMEDIATES
Volume 43, Issue 5, Pages 3121-3130

Publisher

SPRINGER
DOI: 10.1007/s11164-016-2814-2

Keywords

Hantzsch reaction; Acridine-1,8-dione; Hexahydroquinoline; Potassium dihydrogen phosphate; Aqueous ethanol

Funding

  1. National Natural Science Foundation of China [21403100]
  2. National Natural Science Foundation of Liaoning Province
  3. Doctoral Scientific Research Foundation [20141100]

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A simple, clean, and economical methodology for the synthesis of acridine-1,8-dione and hexahydroquinoline derivatives via Hantzsch-type condensation has been described. This study highlights the development of a new green pathway for the preparation of substituted 1,4-dihydropyridines derivatives. The mild, cheap, and nontoxic potassium dihydrogen phosphate (KH2PO4) is proved to be an efficient catalyst for the above multi-component reaction to get excellent yields. Widely available and mostly benign catalyst, eco-friendly solvent, and easy purification are among the several attractive features.

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