1,3-Bis(carboxymethyl)imidazolium Chloride as a Sustainable, Recyclable, and Metal-Free Ionic Catalyst for the Biginelli Multicomponent Reaction in Neat Condition
Prabhakara Madivalappa Davanagere, Barnali Maiti
Abstract
)-one/thiones in the synthesis step with yields of up to 96%. In addition, we synthesized the commercially available drug Monastrol by employing this methodology. The new synthesis method employs the benefits of a broad substrate scope, short reaction time, and high atom economy along with low catalyst loading in neat conditions, and is devoid of chromatographic purification. The ionic salt [BCMIM][Cl] was recycled and reused up to six cycles without substantial damage of its catalytic efficiency.
Topics & Concepts
CatalysisThioureaBiginelli reactionChemistrySalt (chemistry)Ionic liquidChlorideAtom economyIonic bondingSubstrate (aquarium)UreaGreen chemistryOrganic chemistryInorganic chemistryIonGeologyOceanographyMulticomponent Synthesis of HeterocyclesSynthesis and biological activitySynthesis of Tetrazole Derivatives