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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883168Generated: November 2, 2026

4-Methylbenzoyl Chloride → (1-benzenesulfonyl-1H-pyrrol-2-yl)(4-methylphenyl)ketone

https://huagongshe.com/reaction/1883168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylbenzoyl ChlorideHCID 13405—
Reactant1-PhenylsulfonylpyrroleHCID 140146—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,1-DichloroethaneHCID 6365—
Product(1-benzenesulfonyl-1H-pyrrol-2-yl)(4-methylphenyl)ketoneHCID 22928710105.1%

Reaction Steps

Under nitrogen atmosphere, to a suspension of aluminum chloride (4.62 g) in dichloroethane (50 mL) was added a solution of p-toluoyl chloride (4.91 g) in dichloroethane (5 mL) at room temperature over a period of 10 minutes. After stirring for 30 minutes, to the mixture was added a solution of 1-benzenesulfonyl-1H-pyrrole (6.00 g) in dichloroethane (10 mL) over a period of 10 minutes. The mixture was stirred at room temperature for 2 hours, and the reaction mixture was poured into ice water, and the aqueous layer was extracted twice with methylene chloride. The organic layers were combined, dried, filtered and concentrated. The residue was purified by silica gel column chromatography to give (1-benzenesulfonyl-1H-pyrrol-2-yl) (4- methyl-phenyl) ketone (9.9 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759429B2
Source datasetuspto-grants-2004_07
ORD IDord-d334bf9696304121b91235b0e4a831c7
Source noteuspto-grants-2004_07