HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167978Generated: October 26, 2026
Boron trifluoride → 1-Benzenesulfonyl-2-(4-fluorobenzoyl)pyrrole
https://huagongshe.com/reaction/1167978
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | 1-Phenylsulfonylpyrrole | HCID 140146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Benzenesulfonyl-2-(4-fluorobenzoyl)pyrrole | HCID 21972905 | 33% |
Reaction Steps
To a solution of 4-fluorobenzoylchloride (1.74 g, 11 mmol) in dichloromethane (2 ml) was added dropwise a solution of boron trifluoride diethyletherate (3.4 ml, 27.6 mmol) in dichloromethane (20 ml). The mixture was stirred for 10 minutes at room temperature. Subsequently, to the mixture was added dropwise a solution of 1-benzenesulfonylpyrrole (1.9 g, 9.2 mmol) in accordance with a method described in Example 8 (1) in dichloromethane (5 ml). The mixture was stirred for 12 hours. The reaction mixture was poured into ice-water and extracted with ethylacetate. The extract was washed with water and dried. The solvent was evaporated. The obtained crude crystal was recrystallized from isopropylether to give 1-benzenesulfonyl-2-(4-fluorobenzoyl)pyrrole (1.0 g) as a crystal. Yield: 19.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620841B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-417490e6bfb1404886152f4839f0b2be |
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| Source note | uspto-grants-2003_09 |
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