Microwave Activated Synthesis of 2-Imidazolin-5-ones Using Phenyl Isothiocyanate as Cyclocondensing Agent
Corresponding Author(s) : PRADEEP K. TRIPATHY
Asian Journal of Chemistry,
Vol. 19 No. 1 (2007): Vol 19 Issue 1
Abstract
The cyclocondensation reaction of N-acetyl and N-benzoylglycines (1a, b) with aromatic aldehydes in the presence of phenyl isothiocyanate as cyclizing agent and pyridine as a catalyst in an open vessel under microwave irradiation in dry media yielded 4-(arylmethylene)-1-phenyl-2-styryl- and 4-(arylmethylene-1,2-diphenyl-2-imidazolin-5-ones (2f and 2a-e, respectively). It is noteworthy that the reaction is completed within 10 min with much better yields. All the steps are carried out in one pot.
Keywords
Phenyl isothiocyanate
Microwave activation
Cyclocondensation
Green chemistry
1,2-Disubstituted 2-imidazolin-5-ones
K. TRIPATHY, P. (2010). Microwave Activated Synthesis of 2-Imidazolin-5-ones Using Phenyl Isothiocyanate as Cyclocondensing Agent. Asian Journal of Chemistry, 19(1), 813–815. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/20564
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