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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500181Generated: October 25, 2026

Pyrrolidine → 1-[(4-Bromophenoxy)acetyl]pyrrolidine

https://huagongshe.com/reaction/500181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantOxalyl chlorideHCID 65578—
Reactantp-Bromophenoxyacetic acidHCID 74657—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-[(4-Bromophenoxy)acetyl]pyrrolidineHCID 787679—

Reaction Steps

Oxalyl chloride (0.5 mL, 5.9 mmol) was added to a suspension of (4-bromophenoxy)acetic acid (0.462 g, 2.0 mmol) in methylene chloride (10 mL) and 2 drops of N,N-dimethylformamide. The mixture was stirred at RT for 2 h. The solvent was evaporated under reduced pressure. The residue was diluted with methylene chloride (10 mL), cooled with ice-water bath, and 1M of sodium hydroxide aqueous solution (3.0 mL) was added. To the mixture was added pyrrolidine (167 μL, 2.0 mmol). The mixture was stirred and allowed to warm to RT. The organic layer was separated, washed with water and brine, dried over Na2SO4, filtered, and concentrated. The residue was directly used in next step without further purification (550 mg, 96.7%). LCMS: (M+H)=286.0/284.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-746b17a2070148b2ad2b77f13ddfa069
Source noteuspto-grants-2010_08