An efficient synthesis of 4-aryl-7-benzylidene-hexahydro-2H-cyclopenta[d] pyrimidin-2-ones/thiones catalyzed by p-dodecylbenzenesulfonic acid
الموضوعات : Iranian Journal of CatalysisKrishnamoorthy Aswin 1 , Majid Ghashang 2 , Sheik Mansoor 3
1 - Research Department of Chemistry, C. Abdul Hakeem College, Melvisharam – 632 509, India
2 - Faculty of Sciences, Najafabad Branch, Islamic Azad University, Najafabad, Esfahan, Iran
3 - C. Abdul Hakeem College
Bio active Organic Molecule Synthetic Unit, Research Department of Chemistry, Melvisharam - India
الکلمات المفتاحية: Biginelli reaction, One-pot synthesis, p-Dodecylbenzenesulfonic acid, Cyclopenta[d]pyrimidin-2-one,
ملخص المقالة :
A new and efficient method has been developed for the synthesis of 4-aryl-7-benzylidene-1,3,4,5,6,7-hexahydro-2H-cyclopenta[d]pyrimidin-2-ones through Biginelli-like reaction of cyclopentanone, with urea/thiourea and aromatic aldehyde employing p-dodecylbenzenesulfonic acid (DBSA) as a recyclable catalyst under solvent-free condition. The recovered catalyst was recycled for further runs. The product formation takes place via a cross-aldol condensation of benzaldehyde with cyclopentanone in the presence of DBSA to produce benzylidene intermediate and subsequent Michael addition. The present approach offers the advantages of short reaction time, mild reaction conditions, high yields and convenient operation. All the products were obtained in good to excellent yields and the structures of the synthesized compounds were established by advanced spectroscopic data.
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