Coumarin synthesis via knoevenagel condensation reaction in 1,1,3,3-N,N,N',N'- tetramethylguanidinium trifluoroacetate ionic liquid

Abstract

Coumarin derivatives were synthesized in relatively high yields via Knoevenagel condensation reaction of an orthohydroxyaryl aldehyde and an activated β-dicarbonyl C-H acid in the presence of a recyclable ionic liquid 1,1,3,3-N,N,N',N'-tetramethylguanidinium trifluoroacetate under either classical heating conditions or using microwave irradiation. Application of microwave irradiation decreased the required time by a factor of about 200. The ionic liquid could be recycled several times without loss of efficiency with regards to the reaction times and yields.