Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736458Generated: October 29, 2026

p-Bromobenzenesulfonyl chloride → 1-(4-Bromobenzene-1-sulfonyl)pyrrolidine

https://huagongshe.com/reaction/736458

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantSodium HydroxideHCID 14798—
ReactantPyrrolidineHCID 31268—
SolventDichloromethaneHCID 6344—
Product1-(4-Bromobenzene-1-sulfonyl)pyrrolidineHCID 73861898%

Reaction Steps

Pyrrolidine (2.5 g, 35.2 mmol) was added to a solution of 4-bromobenzenesulfonyl chloride (4.5 g, 17.6 mmol) in methylene chloride (10 mL) at 0° C. The mixture was stirred for 2 h and an aqueous sodium hydroxide solution (1 M, 5 mL) was added and stirring was continued for another 10 min. The organic phase was separated and diluted with methylene chloride (40 mL), washed with aqueous HCl (1 M, 10 mL), and water (2×10 mL). The organic phase was dried (sodium sulphate) and the solvent was evaporated. The title compound was isolated in 5.0 g (98% yield) as a white solid: 1H NMR (CDCl3, 400 MHz) δ 7.65 (m, 4H), 3.20 (m, 4H), 1.74 (m, 4H); 13C NMR (CDCl3, 100 MHz) δ 135.93, 132.17, 128.84, 127.39, 47.84, 25.13; MS (ES) m/z 290 and 292 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595321B2
Source datasetuspto-grants-2009_09
ORD IDord-b87fe7c7ac3d4e4c99959dd950ec6ed0
Source noteuspto-grants-2009_09