p-Toluenesulfonic acid → 1-(3-Dimethylaminophenyl)-2-methyl-5-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester

Participants

Reaction Steps

N,N-dimethyl-1,3-phenylenediamine dihydrochloride (5 mmol, 1.09), triethylamine (10 mmol, 1.4 mL), 3-oxo-2-(2-oxo-2-phenyl-ethyl)-butyric acid ethyl ester (5 mmol, 1.2 g), and tosic acid (0.1 g) were combined in ethanol (25 mL), then heated under reflux (12 hrs). The solvents were removed under vacuum, the resulting oil was redissolved in methylene chloride, then applied to a silica column. The purified product was collected as a translucent oil. The named compound was identified by 1H-NMR (CDCl3, ppm) 1.28 t (3H) , 2.35 s (3H) , 2.77 s (6H) , 4.2 q (2H) , 6.3-6.7 m (4H), and 7.0-7.3 m (5H).

Provenance & Evidence