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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278548Generated: October 25, 2026

4-(Chloromethyl)benzoyl chloride → 1-(4-Chloromethylbenzoyl)-4-(2-naphthalenesulfonyl)piperazine

https://huagongshe.com/reaction/278548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)benzoyl chlorideHCID 70136—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Naphthalene-2-sulfonyl)piperazine hydrochlorideHCID 22721815—
SolventEthyl AcetateHCID 8857—
Product1-(4-Chloromethylbenzoyl)-4-(2-naphthalenesulfonyl)piperazineHCID 1105904678%

Reaction Steps

To a mixture of 1-(2-naphthalenesulfonyl)piperazine hydrochloride (5.0 g) in ethyl acetate (60 ml) and an aqueous solution of 10% sodium hydrogen carbonate (40 ml) was added 4-chloromethylbenzoylchloride (3.02 g), and the solution was stirred at room temperature for 30 minutes. The organic layer was separated, washed with water and saturated sodium chloride, dried and concentrated. The residue was washed with diisopropylether and dried under reduced pressure to give the title compound (4.945 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359134B1
Source datasetuspto-grants-2002_03
ORD IDord-832a1a517c664007b64f7f43ee36d6e3
Source noteuspto-grants-2002_03