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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582271Generated: October 30, 2026

Allyl bromide → 1-Allylpiperazine

https://huagongshe.com/reaction/1582271

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 numberUS06734191B2
Source datasetuspto-grants-2004_05
ORD IDord-af7f9b384cf8450fb69bbc6a0a4b482c
Source noteuspto-grants-2004_05