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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868081Generated: November 2, 2026

4-Chlorobenzenesulfonyl chloride → 1-[(4-Chlorophenyl)sulfonyl]-4-[4-fluoro-2-(trifluoromethyl)phenyl]piperazine

https://huagongshe.com/reaction/1868081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(4-Fluoro-2-(trifluoromethyl)phenyl)piperazineHCID 57979759—
SolventDichloromethaneHCID 6344—
Product1-[(4-Chlorophenyl)sulfonyl]-4-[4-fluoro-2-(trifluoromethyl)phenyl]piperazineHCID 6855204469.2%

Reaction Steps

Sulfonylation of 1-(4-fluoro-2-(trifluoromethyl)phenyl)piperazine (386 mg, 1.55 mmol) with 4-chlorobenzene-1-sulfonyl chloride (328.2 mg, 1.555 mmol) was carried out according to the representative sulfonation procedure described in Example 1 using anhydrous dichloromethane (3 mL) as solvent and diisopropylethylamine (1.35 mL, 7.775 mmol) as base. 1-[(4-chlorophenyl)sulfonyl]-4-[4-fluoro-2-(trifluoromethyl)phenyl]piperazine was obtained in 69.2% yield (455 mg) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632838B2
Source datasetuspto-grants-2009_12
ORD IDord-6a09b727c4d74ca2ac3312bfcaa4e280
Source noteuspto-grants-2009_12