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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486508Generated: October 27, 2026

Propargyl bromide → 1-Ethyl-4-(prop-2-ynyl)piperazine

https://huagongshe.com/reaction/1486508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
Reactant1-EthylpiperazineHCID 79196—
SolventAcetoneHCID 180—
Product1-Ethyl-4-(prop-2-ynyl)piperazineHCID 21190741—

Reaction Steps

To the 1-ethylpiperazine (2.33 g, 20.2 mmol) and K2CO3 (2.79 g, 20.2 mmol) in acetone (27 ml) was added propargyl bromide (2.00 g, 13.5 mmol) dropwise at 0° C. under N2. The reaction was stirred at room temperature overnight. The reaction was filtered and the salts washed with a small amount of acetone. The filtrates were combined and evaporated gently to concentration. The residue was taken up in EtOAc and washed with water. The aqueous phase was re-extracted with EtOAc. The combined organic layers were washed with brine and dried over MgSO4. The product was filtered and evaporated to dryness to leave a pale orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428439B2
Source datasetuspto-grants-2016_08
ORD IDord-1aecab577c21433f8f76a6b004c2785f
Source noteuspto-grants-2016_08