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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantPotassium CarbonateHCID 11430—
Reactant1-MethylpiperazineHCID 53167—
SolventWaterHCID 962—
Product1-((4-Fluorophenyl)sulfonyl)-4-methylpiperazineHCID 76791437%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415359B2
Source datasetuspto-grants-2013_04
ORD IDord-e1ab29b40b624dad829448dbc6e65db4
Source noteuspto-grants-2013_04