Abstract A highly efficient protocol has been developed for the synthesis of aminals from γ- butyrolactam and benzaldehyde using iodine as Lewis acid catalyst. The attack of γ- butyrolactam nucleophile to intermediate N-acyliminium ion was more favorable, when aryl aldehyde bears the electron donating group (EDG). Iodine plays a key role in these reaction transformations. This current mild protocol is environmentally benign and cost-effective ...