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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435684Generated: October 26, 2026

HCID 21481138, compound → 3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinone

https://huagongshe.com/reaction/435684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21481138HCID 21481138—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-[2-(1-Piperazinyl)ethyl]-2-oxazolidinoneHCID 12275545—

Reaction Steps

291 g of 3-[2-(4-benzyl-1-piperazinyl)-ethyl]-2-oxazolidinone dihydrochloride in 7 litres of methanol are hydrogenated in the presence of 70 g of palladium/carbon (5%) at 50° C and 10 atmospheres of hydrogen. The mixture is filtered and concentrated under reduced pressure. The residue is treated with sodium hydroxide, extracted with chloroform, filtered through diatomaceous earth and concentrated. There is obtained 3-[2-(1-piperazinyl)-ethyl]-2-oxazolidinone as a yellow oil. The dihydrochloride of melting point 203° C (decomposition) is obtained by treatment with an excess of hydrochloric acid in methanol/ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006144
Source datasetuspto-grants-1977_02
ORD IDord-a46e1198afdf4f44b01fa1b4f0dae01f
Source noteuspto-grants-1977_02