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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253664Generated: November 3, 2026

HCID 15158302, compound → HCID 15034745, compound

https://huagongshe.com/reaction/2253664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15158302HCID 15158302—
CatalystHCID 178418390HCID 178418390—
SolventAcetic AcidHCID 176—
ProductHCID 15034745HCID 15034745—

Reaction Steps

A solution of 4.87 g of 1-(3-p-methoxyphenyloxazolidin-2-one-5-yl-methyl)-4-(3,4-methylenedioxyphenyl)pyridinium bromide [obtainable from 3-p-methoxyphenyl-5-bromomethyloxazolidin-2-one and 4-(3,4-methylenedioxyphenyl)pyridine] in 60 ml of acetic acid is hydrogenated over 1 g of 10% strength Pd/carbon at 20° and atmospheric pressure until the absorption of hydrogen has ceased. After filtration, evaporation and usual workup, 3-p-methoxyphenyl-5-[4-(3,4-methylenedioxyphenyl)piperidinomethyl]oxazolidin-2-one is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05232931
Source datasetuspto-grants-1993_08
ORD IDord-f231c72cc06f461a929d150304fa1f9a
Source noteuspto-grants-1993_08