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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387017Generated: October 30, 2026

Pyrrolidine → 1-(4-Bromobenzyl)pyrrolidine

https://huagongshe.com/reaction/1387017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant4-Bromobenzyl bromideHCID 68527—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-(4-Bromobenzyl)pyrrolidineHCID 1273800494%

Reaction Steps

Pyrrolidine (20.0 mL, 0.240 mole) was added to a stirred solution of 4-bromobenzyl bromide (10.0 g, 40.0 mmol) in anhydrous CH2Cl2 (20 mL) at 0° C. under nitrogen. The resultant solution was allowed to stir at room temperature for 1 h. The reaction mixture was diluted with EtOAc (150 mL) before it was washed with half-saturated aqueous NaHCO3 (50 mL). After drying over MgSO4, filtration, and concentration, the oily residue was chromatographed on silica [20% EtOAc in hexanes, then 10% EtOH/Et3N (2/1) in THF/hexanes (1/1)] to provide 9.02 g of the benzyl pyrrolidine (94%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-6b4c5f1dd995414b9a36e7cfa2201a4a
Source noteuspto-grants-2001_07