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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157875Generated: November 2, 2026

Allyl bromide → 1-Allylpiperazine

https://huagongshe.com/reaction/1157875

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 numberUS07807694B2
Source datasetuspto-grants-2010_10
ORD IDord-e2efc3b16592426080f85388a6ca69ce
Source noteuspto-grants-2010_10