344871-28-9

Upstream product

• 81454-02-6 4-<1-(Phenylsulfonyl)-3-pyrrolyl>-4-oxobutyric acid 
• 16851-82-4 N-phenylsulfonylpyrrole 
• 86688-99-5 4-<1-(Phenylsulfonyl)-3-pyrrolyl>butyric acid 

Downstream Products

• 86689-00-1 1-(phenylsulfonyl)-1,4,5,6-tetrahydro-7H-indol-7-one 
• 23456-78-2 1,4,5,6-tetrahydro-7H-indol-7-one 

Relevant academic research and scientific papers

Regioselective Synthesis of Acylpyrroles

The regioselective synthesis of several pyrrole derivatives is described.AlCl3-catalyzed acylation reactions of 1-(phenylsulfonyl)pyrrole (1) give 3-acyl derivatives, whereas the corresponding BF3*OEt2-catalyzed reactions give 2-acyl derivatives predominantly.Mild alkaline hydrolysis gives the corresponding acyl-1H-pyrroles in excellent yields.AlCl3-catalyzed reactions of 1 with 1,1-dichloromethyl methyl ether and oxalyl chloride give 1-(phenylsulfonyl)-2-formylpyrrole (6) and 1-(phenylsulfonyl)-2-(chlorocarbonyl)pyrrole (7), respectively. 3-Pyrrolylacetic acid (10) was prepared by thallium(III) nitrate promoted rearrangement of 1-(phenylsulfonyl)-3-acetylpyrrole (2a).Trifluoroacetic anhydride catalyzed cyclization of 4-butyric acid (14) gives 1-(phenylsulfonyl)-7-oxo-4,5,6,7-tetrahydroindole (17).Attempts to cyclize 14 at the 4-position have been unsuccessful.