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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916481Generated: October 29, 2026

2-Bromoethanol → 2-[4-(2-Fluoroethyl)piperazin-1-YL]ethanol

https://huagongshe.com/reaction/916481

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
ReactantEthanol, 1-bromo-HCID 14202443—
ReactantHCID 87238377HCID 87238377—
SolventAcetonitrileHCID 6342—
Product2-[4-(2-Fluoroethyl)piperazin-1-YL]ethanolHCID 4509964966.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

1-(2-Fluoroethyl)piperazine diTFA salt (464 mg, 1.29 mmol), (prepared as described for the starting material in Example 27), was dissolved in acetonitrile (3.5 ml). Potassium carbonate (889 mg, 6.44 mmol) and 2-bromoethanol (95 μl, 1.34 mmol) were added and the mixture heated to 85° C. and left overnight. More bromoethanol (95 μl, 1.34 mmol) was added and the reaction mixture heated at 85° C. for a further 2 hours. The reaction mixture was cooled, filtered and concentrated. The residue was purified by column chromatography eluting with methylene chloride/methanol (saturated with ammonia) (92/8) to give 2-[4-(2-fluoroethyl)piperazin-1-yl]ethanol (151 mg, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268230B2
Source datasetuspto-grants-2007_09
ORD IDord-8ef5f226b33742daa00b5744de1794bc
Source noteuspto-grants-2007_09