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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400587Generated: October 25, 2026

Benzenesulfonyl chloride → N,N-bisbenzenesulfonyl-(4-bromo-2-iodoaniline)

https://huagongshe.com/reaction/400587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant4-Bromo-2-iodoanilineHCID 823934—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductN,N-bisbenzenesulfonyl-(4-bromo-2-iodoaniline)HCID 6002685035%

Reaction Steps

A solution of 4-bromo-2-iodoaniline (8.5 g, 28.5 mmol) in 200 mL of dichloromethane was sequentially treated with benzenesulfonyl chloride (15 mL, 117.5 mmol) and triethylamine (25 mL, 179.6 mmol). After 4 days, the mixture was diluted with 100 mL of saturated aqueous sodium bicarbonate solution and extracted with three 100 mL portions of ethyl acetate. The combined organic layers were washed with 50 mL of brine, three 60 mL portions of saturated aqueous ammonium chloride solution, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude product was triturated with diethyl ether to afford 5.74 g (35% yield) of N,N-bisbenzenesulfonyl-(4-bromo-2-iodoaniline).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741897B2
Source datasetuspto-grants-2014_06
ORD IDord-53ca051e0a414058a5925be0c353bd28
Source noteuspto-grants-2014_06