HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964699Generated: October 30, 2026
4-Fluorobenzenesulfonyl chloride → 1-((4-Fluorophenyl)sulfonyl)-4-methylpiperazine
https://huagongshe.com/reaction/1964699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-((4-Fluorophenyl)sulfonyl)-4-methylpiperazine | HCID 767914 | 37% |
Reaction Steps
Commercially available 4-fluorobenzenesulfonyl chloride (1.00 g, 5.14 mmol) was suspended in water (15 mL), and N-methylpiperazine (0.68 mL, 6.17 mmol) and potassium carbonate (1.56 g, 11.3 mmol) were added, followed by stirring at room temperature for 14 hours under nitrogen atmosphere. To the reaction solution, water (50 mL) was added, followed by extraction with ethyl acetate (50 mL), and subsequently the organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified using silica gel column chromatography (elution solvent: ethyl acetate/hexane=50%-90%) to afford the desired compound (491 mg, yield 37%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415359B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-e1ab29b40b624dad829448dbc6e65db4 |
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| Source note | uspto-grants-2013_04 |
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