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A rapid and efficient, one pot synthesis of spirooxindole derivatives has been attempted by threecomponent reaction of isatin, malononitrile and carbonyl compound possessing a reactive a-methylene group by using task specific ionic liquid, 1-butyl-3-methyl imidazolium hydroxide [bmim]OH as a catalyst. The important features of this methodology are straight forward route in short reaction time at room temperature and avoid any hazardous organic solvent, toxic catalyst, tedious purification step.Interestingly, this protocol is not only limited to mono-systems but also to the synthesis of newer bisspirooxindole system. The separation of the product and reusability of the catalyst are easy with excellent yield. The [bmim]OH catalyst system could be reused up to five recycles without appreciable loss of activity.
A rapid and efficient, one pot synthesis of spirooxindole derivatives has been attempted by threecomponent reaction of isatin, malononitrile and carbonyl compound possessing a reactive a-methylene group by using task specific ionic liquid, 1-butyl-3-methyl imidazolium hydroxide [bmim] OH as a catalyst. The important features of this methodology are straightforward route in short reaction time at room temperature and avoid any hazardous organic solvent, toxic catalyst, tedious purification step. Interestingly, this protocol is not only limited to mono-systems but also The synthesis of newer bisspirooxindole system. The separation of the product and reusability of the catalyst are easy with excellent yield. The [bmim] OH catalyst system could be reused up to five recycles without appreciable loss of activity.