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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8933Generated: October 25, 2026

Allyl bromide → 1-Allylpiperazine

https://huagongshe.com/reaction/8933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantTrifluoroacetylpiperazineHCID 7172020—
SolventAcetonitrileHCID 6342—
Product1-AllylpiperazineHCID 806422155.1%

Reaction Steps

To a stirred solution of 2,2,2-trifluoro-1-piperazin-1-yl-ethanone (515 mg, 2.83 mmol) in dry CH3CN (6 mL) was added allyl bromide (0.32 mL, 3.7 mmol) and powdered potassium carbonate (0.78 g, 5.65 mmol) and the mixture stirred overnight. The reaction was concentrated under reduced pressure, diluted with CH2Cl2 (30 mL) and water (30 mL) and the aqueous layer extracted with CH2Cl2 (2×20 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo to afford the crude di-protected piperazine (0.554 g) which was used without further purification in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091217B2
Source datasetuspto-grants-2006_08
ORD IDord-32ee4c940d754b23bf862be162c61ba9
Source noteuspto-grants-2006_08