Synthesis of coumarin-3-ethyl formate under microwave irradiation without solvent
Wang Xi-yun
Abstract
Wang Xi-yun
Abstract
Six coumarin-3-ethyl formates were synthesized from substituted salicylaldehyde and diethyl monlonate under microwave irradiation without solvent.The structure of the title compounds were characterized by IR,1H NMR and 13C NMR.The optimum parameters of coumarin-3-ethyl formate were obtained by orthogonal test: microwave power 400 W,reaction time 6 min,ratio of aldehyde to diethyl monalate 1∶1.3 and piperizine 0.3 mL respectively.Under this optimized condition,the yield of the title compounds were 39.2%~85.9% with such advantages as short time,high yields and environmentally benign procedures compared with the traditional methods.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Six coumarin-3-ethyl formates were synthesized from substituted salicylaldehyde and diethyl monlonate under microwave irradiation without solvent.The structure of the title compounds were characterized by IR,1H NMR and 13C NMR.The optimum parameters of coumarin-3-ethyl formate were obtained by orthogonal test: microwave power 400 W,reaction time 6 min,ratio of aldehyde to diethyl monalate 1∶1.3 and piperizine 0.3 mL respectively.Under this optimized condition,the yield of the title compounds were 39.2%~85.9% with such advantages as short time,high yields and environmentally benign procedures compared with the traditional methods.
Key concepts: Coumarin, Ethyl formate, Salicylaldehyde, Yield (engineering), Solvent, Formate, Proton NMR, Microwave irradiation