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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856455Generated: November 4, 2026

1-Phenylpiperazine → HCID 23345032, compound

https://huagongshe.com/reaction/1856455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantHCID 23345057HCID 23345057—
SolventMethanolHCID 887—
ProductHCID 23345032HCID 2334503261%

Reaction Steps

15.5 millimoles of 4-[3-(2,3-epoxypropoxy)-4-methoxyphenyl]-2-pyrrolidone is dissolved in 50 ml. of methanol. After the addition of 15.5 mmol of 1-phenylpiperazine (95% strength), the reaction mixture is heated for 3 hours under reflux. After cooling of the reaction solution, the solvent is removed under vacuum at 40°. The residue is taken up in 50 ml. of 1N hydrochloric acid and extracted twice with 100 ml. of chloroform. The aqueous phase is adjusted to be alkaline with 2N sodium hydroxide solution and thereafter extracted three times with ethyl acetate. The combined ethyl acetate phase are washed with saturated sodium chloride solution, and the solvent, after drying over sodium sulfate, is distilled off under vacuum. The residue is recrystallized from ethanol, thus obtaining in a 61% yield 4-{4-methoxy-3-[3-(4-phenylpiperazin-1-yl)-2-hydroxypropoxy ]phenyl}-2-pyrrolidone, m.p. 143°-144°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04219551
Source datasetuspto-grants-1980_08
ORD IDord-5f2da4f80fcf4f1c803468463369e82f
Source noteuspto-grants-1980_08