Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283375Generated: October 31, 2026

Triethylamine → (E)-4-Chloro-2-(2-(3,4-dichlorophenyl)vinylsulfonamido)benzenesulfonamide

https://huagongshe.com/reaction/2283375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-4-chlorobenzenesulphonamideHCID 77790—
Reactant(E)-2-(3,4-dichlorophenyl)ethenesulfonyl chlorideHCID 22719686—
SolventDichloromethaneHCID 6344—
Product(E)-4-Chloro-2-(2-(3,4-dichlorophenyl)vinylsulfonamido)benzenesulfonamideHCID 5775090391.5%

Reaction Steps

2-Amino-4-chlorobenzenesulfonamide (100 mg, 0.48 mmol) and (E)-2-(3,4-dichlorophenyl)ethenesulfonyl chloride (171 mg, 0.63 mmol) were dissolved in anhydrous dichloromethane (5 mL) and were flushed with argon. Anhydrous triethylamine (0.155 mL, 1.11 mmol) was added and the reaction was stirred at room temperature under an inert atmosphere over night. The reaction was quenched using 2 M hydrochloric acid (20 mL) and extracted with dichloromethane. The combined organic phases were washed with water, dried over magnesium sulfate and concentrated under vacuum to give 194 mg (91% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-bd24960907dd4c8485d631ba43c33bd7
Source noteuspto-grants-2015_09