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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417993Generated: October 26, 2026

Oxalyl chloride → 3-Bromo-1-(4-fluorophenyl)piperazine 2,2-dimethylpropan-1-one

https://huagongshe.com/reaction/417993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Bromo-2,2-dimethylpropanoic acidHCID 271932—
SolventDichloromethaneHCID 6344—
Product3-Bromo-1-(4-fluorophenyl)piperazine 2,2-dimethylpropan-1-oneHCID 8663578084%

Reaction Steps

3-Bromo-2,2-dimethylpropionic acid (5.03 g, 27.8 mmol) was dissolved in DCM (60 mL). Oxalyl chloride (3.64 mL, 41.67 mmol) was added slowly over 10 minutes. The reaction mixture was stirred at room temperature for 18 hours and then concentrated in vacuo. The residue was dissolved in DCM (40 mL) and added to a solution of 4-fluorophenyl-piperazine (5.00 g, 27.8 mmol) and DIPEA (7.24 mL, 41.67 mmol) in DCM (30 mL) at 0° C. The reaction mixture was allowed to warm to room temperature over 1 hour and then stirred at room temperature for 16 hours. The reaction mixture was washed with 10% citric acid solution (2×100 mL), dried (MgSO4) and concentrated in vacuo to give 3-bromo-1-(4-fluorophenyl)piperazine-2,2-dimethylpropan-1-one (8.04 g, 84%) as a yellow solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093248B2
Source datasetuspto-grants-2012_01
ORD IDord-03b004c3c8914e32964d2d6eb8016ce7
Source noteuspto-grants-2012_01