The cyclic intermediate undergoes an aromatic nucleophilic substitution reaction to form the final 1,2-disubstituted indole. This step involves the attack of the nitrogen atom in the cyclic intermediate on the carbon adjacent to the halogen in the aromatic ring.
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2-(4-chlorophenyl)-1-(p-tolyl)-1H-indole
sulfuric acid
Ethyl acetate
4,4'-Methylenebis(2,3,5,6-tetramethylphenol)
