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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992350Generated: October 30, 2026

Triethylamine → N-(2-bromoethyl)-4-fluorobenzenesulfonamide

https://huagongshe.com/reaction/1992350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactant2-Bromoethylamine hydrobromideHCID 2774217—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(2-bromoethyl)-4-fluorobenzenesulfonamideHCID 2779738—

Reaction Steps

4-Fluoro benzene sulfonyl chloride (8 g, 0.0411 mol) was added dropwise at 0° C. to a solution of 2-bromoethylamine hydrogen bromide (10.27 g, 0.0501 mol) and triethyl amine (14.3 ml, 0.1029 mol) in dry dichloromethane (100 ml) and stirred at room temperature for 1 h under nitrogen atmosphere. The reaction mixture was diluted with water and extracted with ethyl acetate. Organic layer was washed with water and brine and dried over sodium sulfate. Solvent evaporation under reduced pressure afforded the sub-title product as a liquid. Yield: 11 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648985B2
Source datasetuspto-grants-2010_01
ORD IDord-6c84479aa6cf4876b0bc149ae09b6f2a
Source noteuspto-grants-2010_01