HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31541Generated: October 26, 2026
4-Methylbenzoyl Chloride → 1-(1-Benzenesulfonyl-1H-pyrrol-3-yl)-1-p-tolyl-methanone
https://huagongshe.com/reaction/31541
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 | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-(1-Benzenesulfonyl-1H-pyrrol-3-yl)-1-p-tolyl-methanone | HCID 475639 | 105.3% |
Reaction Steps
Under nitrogen atmosphere, to a suspension of aluminum chloride (4.62 g, 34.7 mmol) in ethylene chloride (50 mL) was added a solution of p-toluoyl chloride (4.91 g, 31.8 mmol) in ethylene chloride (5 mL) at room temperature over a period of 10 minutes. The mixture was stirred for 30 minutes, and thereto was added a solution of 1-benzenesulfonyl-1H-pyrrole (6.00 g, 28.9 mmol) in ethylene chloride (10 mL) over a period of 10 minutes. The mixture was stirred at room temperature for 2 hours. The reaction mixture was poured into ice-water, and the aqueous layer was extracted twice with dichloromethane. The organic layers were combined, dried, and filtered. The filtrate was concentrated, and the residue was purified by silica gel column chromatography to give the title compound (9.9 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425642B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-ba8804115d7f438d8e16948d3df34747 |
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| Source note | uspto-grants-2008_09 |
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