Journal
RSC ADVANCES
Volume 13, Issue 29, Pages 19846-19855Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ra03183g
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A green, efficient, and straightforward method for the synthesis of 2,4,5-triarylimidazole has been developed using unconventional CuB4O7 as a promoter under solvent-free conditions. This approach enables the synthesis of a library of 2,4,5-triarylimidazole compounds. Additionally, the in situ isolation of compounds (5) and (6) provides insight into the direct conversion of CuB4O7 into copper acetate in the presence of NH4OAc under solvent-free conditions. The main advantages of this protocol include easy reaction procedure, short reaction time, and easy work up of the product without the need for tedious separation methods.
A green, efficient, and straightforward methodology for the three-component synthesis of 2,4,5-triarylimidazole has been developed under solvent-free conditions using unconventional CuB4O7 as a promoter. This green approach encouragingly provides access to a library of 2,4,5-tri-arylimidazole. Also, we have been able to isolate the compound (5) and (6) in situ, which provides an insight into the direct conversion of CuB4O7 into copper acetate in the presence of NH4OAc under solvent-free condition. The main advantage of this protocol includes an easy reaction procedure, short reaction time, and easy work up of the product without using any tedious separation method.
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