Green Synthetic Approach to Indole-Substituted Methane Derivatives via Multi-Component Reaction

A one-pot multicomponent synthesis of unsymmetrical indole-substituted methane derivative based on two consecutive reactions of p-methyl-benzaldehyde with N-methylindole and 5,5-dimethyl-1,3-cyclohexane-dione is described as an experiment that was carried out by second-year undergraduate chemistry students individually in a laboratory classroom. The experiment provides an opportunity for students to carry out novel organic chemistry transformations for the synthesis of complex molecules from simple substrates, which is also the main pedagogical goal. Salient features of this teaching experiment include (a) multicomponent synthesis and good operability, (b) the absence of catalyst and any additives, (c) high yield and atomic economy, and (d) the use of inexpensive and green solvent. This laboratory experiment combines organic synthesis, TLC, NMR, and IR analysis. Several important concepts, such as green chemistry, chem- and regioselectivity, conjugated 1,4-addition, and atomic economy, are also discussed.

Automated summary

This experiment involves a one-pot multicomponent synthesis to prepare an unsymmetrical indole-substituted methane derivative using two consecutive reactions. It was conducted by second-year undergraduate chemistry students in a laboratory classroom. The experiment offers students an opportunity to perform novel organic chemistry transformations and synthesize complex molecules from simple substrates. The experiment has several noteworthy features, including multicomponent synthesis, good operability, absence of catalyst and additives, high yield and atomic economy, and the use of inexpensive and green solvent. It also incorporates various analytical techniques such as TLC, NMR, and IR analysis, and discusses important concepts such as green chemistry, chem- and regioselectivity, conjugated 1,4-addition, and atomic economy.