Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360593Generated: October 30, 2026

Phenethyl bromide → 4-(2-Bromoethyl)benzenesulfonyl chloride

https://huagongshe.com/reaction/2360593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantChlorosulfonic acidHCID 24638—
SolventChloroformHCID 6212—
Product4-(2-Bromoethyl)benzenesulfonyl chlorideHCID 1284677580.6%

Reaction Steps

To a solution of 2-bromoethylbenzene (10.0 g; 54 mmol) in 16 ml of chloroform placed at a temperature of 0° C. was added dropwise a solution of chlorosulfonic acid (162 mmol, 18.87 g; 10.82 ml) in 11 ml of chloroform. After 15 minutes at 0° C., the reaction was maintained at room temperature for 3 hours. The reaction mixture was poured onto ice, and the aqueous phase was extracted with chloroform. The combined organic phases were washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated off to give 12.34 g of crude product, which was purified by chromatography on a column of silica, eluting with chloroform (76% yield). The product obtained was used for the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686147B2
Source datasetuspto-grants-2014_04
ORD IDord-32f1c94e187f430c8540b35bf68c0823
Source noteuspto-grants-2014_04