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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791863Generated: November 3, 2026

Hydrochloric Acid → N-{3-[2-(4-Cyanophenyl)ethylthio]phenyl}benzenesulfonamide

https://huagongshe.com/reaction/1791863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantAmino-3-[2-(4-cyanophenyl)ethylthio]benzeneHCID 22033546—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-{3-[2-(4-Cyanophenyl)ethylthio]phenyl}benzenesulfonamideHCID 2203348382.1%

Reaction Steps

Benzenesulfonyl chloride (0.62 g; 3.5 mmol) was added to a cold solution (ice:water temperature) of amino-3-[2-(4-cyanophenyl)ethylthio]benzene (0.80 g; 3.15 mmol; from step (ii) above) in a mixture of pyridine (1 mL) and CH2Cl2 (20 mL) over 10 minutes. After 3 hours stirring, 2M aqueous HCl was added and the solution extracted with CH2Cl2. The organic layer was dried (MgSO4) and the solvent removed in vacuo. The residue was purified by flash chromatography (SiO2; Et2O:hexane (1:1)) to give 1.02 g (82%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074820B2
Source datasetuspto-grants-2006_07
ORD IDord-900bd1dae3d14db3a3e119f5d642c9f2
Source noteuspto-grants-2006_07