4.4 Article

Synthesis of 4H-Benzopyrans Catalyzed by Acyclic Acidic Ionic Liquids tin Aqueous Media

Journal

JOURNAL OF HETEROCYCLIC CHEMISTRY
Volume 47, Issue 1, Pages 63-67

Publisher

WILEY
DOI: 10.1002/jhet.254

Keywords

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Funding

  1. Educational Commission of Jiangsu Province [07KJD530238]
  2. Jiangsu Provincial Key Laboratory of Coastal Wetland Bioresources & Environmental Protection [JLCBE 09023]

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Some halogen-free acyclic task-specific ionic liquids (TSILs) were synthesized as novel and recyclable catalysts for the synthesis of 5-oxo-5,6,7,8-tetrahydi-o-4H-benzo[b]pyrans by one-pot three-component condensation of aromatic aldehyde, malononitrile (or ethyl cyanoacetate), and dimedone (or 1,3-cyclohexanedione) in water. The condensation accomplished successfully with good yields ranged from 86 to 94%. After the reaction, the products could simply be separated from the catalyst/water, and the catalyst could be reused at least 10 times without noticeably decreasing the catalytic activity.

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