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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| Reactant | 1-Phenylsulfonylpyrrole | HCID 140146 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | (1-benzenesulfonyl-1H-pyrrol-2-yl)(4-methylphenyl)ketone | HCID 22928710 | 105.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06759429B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-d334bf9696304121b91235b0e4a831c7 |
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| Source note | uspto-grants-2004_07 |
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