Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287137Generated: October 30, 2026

Piperazine → HCID 3787305, compound

https://huagongshe.com/reaction/2287137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-((4-Chlorophenoxy)methyl)oxiraneHCID 91515—
SolventMethanolHCID 887—
ProductHCID 3787305HCID 3787305—

Reaction Steps

While 9.3 g of piperazine is refluxed in 50 ml of methanol with stirring, 10 g of p-chlorophenyl glycidyl ether are added dropwise over a period of 1.5 hours. After the addition has been completed, the mixture is refluxed with stirring for a further 1.5 hours, and then concentrated to dryness under reduced pressure. The residue is dissolved in dilute hydrochloric acid and extracted with ethyl acetate. The water layer is rendered basic with sodium hydroxide, extracted first with benzene from which there can be obtained N,N'-bis[3-(4-chlorophenoxy)-2-hydroxypropyl]piperazine, and then with n-butanol. The butanol extracts are washed with water and the solvent then removed by distillation under reduced pressure to yield 10.0 g of N-[3-(4-chlorophenoxy)-2-hydroxypropyl]piperazine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04269838
Source datasetuspto-grants-1981_05
ORD IDord-4afb65a9d0d848589c11f3af3cdb6be0
Source noteuspto-grants-1981_05