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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414197Generated: October 26, 2026

Piperazine → 3-Phenyl-1-(piperazin-1-yl)prop-2-en-1-one

https://huagongshe.com/reaction/1414197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant3-Phenylprop-2-enoyl chlorideHCID 66023—
SolventChloroformHCID 6212—
Product3-Phenyl-1-(piperazin-1-yl)prop-2-en-1-oneHCID 28094930%

Reaction Steps

Absolute piperazine (206 g) was dissolved in 500 ml of chloroform and 66.3 g of cinnamoyl chloride was added gradually at 0° C while mixing. The addition required 3 hours. After mixing was continued for another 2 hr., precipitates were filtered and then the filtrate (chloroform layer) was washed with 50 ml of 5% sodium hydroxide and 50 ml of water. The residues obtained after solvents were distilled away in vacuo were subjected to silica gel column chromatography (eluants were mixtures of chloroform and methanol). Thus crystalline N-cinnamoyl piperazine was obtained. Melting point of the product was 30°-40° C and the product was very hygroscopic. The yield was 30%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001223
Source datasetuspto-grants-1977_01
ORD IDord-b6c22d5eb320463f9d9e4c1813b1aa2f
Source noteuspto-grants-1977_01