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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576851Generated: October 26, 2026

Benzenesulfonyl chloride, 4-chloro-3-nitro- → 1-[(4-Chloro-3-nitrophenyl)sulfonyl]-4-methylpiperazine

https://huagongshe.com/reaction/576851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
SolventTetrahydrofuranHCID 8028—
Product1-[(4-Chloro-3-nitrophenyl)sulfonyl]-4-methylpiperazineHCID 2842419—

Reaction Steps

N-methylpiperazine 3.6 mL, N,N-diisopropylethylamine 5.7 mL and tetrahydrofuran 31 mL were mixed and dropped into a solution of 4-chloro-3-nitrobenzenesulfonyl chloride 8.19 g in tetrahydrofuran 51 mL, under cooling with ice, followed by stirring for 30 minutes under cooling with ice. The stirring was then continued for 17 hours at room temperature. The solvent was distilled off and the residue was poured in water, of which pH was raised to 9 with saturated aqueous sodium hydrogencarbonate solution, followed by extraction with ethyl acetate-tetrahydrofuran mixed solvent. The organic layer was washed with saturated brine, dried over magnesium sulfate, and from which the solvent was distilled off. Recrystallizing the crude product from ethyl acetate-hexane mixed solvent, 4.29 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040536B2
Source datasetuspto-grants-2015_05
ORD IDord-77d1100fc0644859b67dc63e193cef25
Source noteuspto-grants-2015_05