Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/13707
Title: A novel catalyst cobalt <i style="">m</i>-nitrobenzenesulfonate-catalyzed highly efficient synthesis of substituted-quinazolin-4(1<i style="">H</i>)-ones
Authors: Song, Zhiguo
Wan, Xin
Zhao, Shuang
Keywords: Benzenesulfonate
Isatoic Anhydride
One-Pot Reaction
Quinazolinones
Issue Date: Mar-2012
Publisher: NISCAIR-CSIR, India
Abstract: A highly efficient synthesis of mono- and disubstituted 2,3-dihydro-quinazolin-4(1<i style="">H</i>)-ones has been performed by the condensation of isatoic anhydride, aldehydes, and ammonium salts or amines in EtOH/H<sub>2</sub>O under reflux. A novel water-tolerant Lewis acid, cobalt <i style="">m</i>-nitrobenzenesulfonate, has been prepared and applied as a favorable catalyst in this one-pot three-component cyclocondensation reaction. The optimal amounts of catalyst and solvent are investigated. Experimental results show that only 3 mol% catalyst is enough to induce the conversion and EtOH/H<sub>2</sub>O [1/3 (v/v)] system is observed as the best choice. All the reactions are performed within a short reaction time and the catalyst is easily recovered and recycled. The structures of new compounds are characterized by IR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, MS and elemental analysis. A mechanism to rationalize the reaction is proposed.
Description: 118-123
URI: http://hdl.handle.net/123456789/13707
ISSN: 0975-0991 (Online); 0971-457X (Print)
Appears in Collections:IJCT Vol.19(2) [March 2012]

Files in This Item:
File Description SizeFormat 
IJCT 19(2) 118-123.pdf96.16 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.