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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416674Generated: November 2, 2026

1-(3-(Trifluoromethyl)phenyl)piperazine → 3-[4-(3-Trifluoromethylphenyl)-1-piperazinyl]propionic acid

https://huagongshe.com/reaction/2416674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
ReactantEthyl 3-bromopropionateHCID 68320—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
Product3-[4-(3-Trifluoromethylphenyl)-1-piperazinyl]propionic acidHCID 1142660575.2%

Reaction Steps

The reaction mixture of 1-(3-trifluoromethylphenyl)piperazine (510 mg, 2.2 mmol), ethyl 3-bromopropionate (500 mg, 2.7 mmol), sodium bicarbonate (300 mg, 3.5 mmol) and ethanol (15 ml) was refluxed for 3 h till the amine disappeared completely. After the mixture was filtered, the resulting solid was dissolved in 5 ml dioxane and 14 ml 5% sodium hydroxide solution. The mixture was stirred at room temperature overnight, then it was acidified with concentrated hydrogen chloride. Solid was filtered and washed with water, and then dried to give 500 mg 3-[4-(3-trifluoromethylphenyl)-1-piperazinyl]propionic acid as a white solid, mp 228-230° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825207B2
Source datasetuspto-grants-2004_11
ORD IDord-147923c766b842b69f30d405e0af3a6f
Source noteuspto-grants-2004_11