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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916580Generated: November 1, 2026

1,4-Dibromobutane → 1-(4-Bromophenethyl)pyrrolidine

https://huagongshe.com/reaction/1916580

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-Bromophenyl)ethan-1-amine--hydrogen chloride (1/1)HCID 19703973—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-(4-Bromophenethyl)pyrrolidineHCID 12177810—

Reaction Conditions

Temperature75 °C

Reaction Steps

0.51 mL (4.23 mmol) 1,4-dibromobutane in 20 mL acetonitrile is added slowly to a solution of 1.0 g (4.23 mmol) 4-bromo-phenethylamine hydrochloride, 1.8 g (13.0 mmol) K2CO3 and 200 mg (1.20 mmol) Kl in 100 mL acetonitrile at 75° C. and the reaction mixture is stirred for a further 4 h at 75° C. The reaction solution is diluted with 100 mL water and the aqueous phase is extracted with 100 mL EtOAc. The combined organic extracts are washed with saturated NaCl solution, the organic phase is dried over Na2SO4 and the solvent is eliminated i.vac. Further purification is carried out by column chromatography on silica gel (EtOAc/MeOH/NH3 9:1:0.1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-488fc83eb3934255bdcf9f36d0e594e6
Source noteuspto-grants-2013_12