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A new green room temperature ionic liquid catalyzes synthesis of monastrol and its derivatives through Biginelli reaction / 第二军医大学学报
Article Dans Zh | WPRIM | ID: wpr-839930
Responsable en Bibliothèque : WPRO
ABSTRACT
Objective To explore an easily-controllable, environmentally-friendly method for synthesizing monastrol and its derivatives. Methods Monastrol and its derivatives were synthesized using (substituted) benzaldehyde, ethyl acetoacetate and thiourea (or urea) as the material through a Biginelli reaction catalyzed by green room temperature ionic liquid 1-buty-3- methylimidazolium-L-camphorsulfonate under microwave irradiation without solvent. Results The green room temperature ionic liquid 1-buty-3-methylimidazolium-L-camphorsulfonate catalyzed Biginelli reaction in obtaining the title compound under microwave irradiation without solvent. The process was easy to operate, time saving and environmentally-friendly. Conclusion Microwave-accelerated solvent-free Biginelli reaction using green room temperature ionic liquid 1-buty-3-methylimidazolium-L- camphorsulfonate as catalyst is a convenient and environmentally-friendly method for synthesizing monastrol and its derivatives.

Texte intégral: 1 Indice: WPRIM langue: Zh Texte intégral: Academic Journal of Second Military Medical University Année: 2011 Type: Article
Texte intégral: 1 Indice: WPRIM langue: Zh Texte intégral: Academic Journal of Second Military Medical University Année: 2011 Type: Article