Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094625Generated: October 27, 2026

m-Chloroperbenzoic acid → Oxymorphone

https://huagongshe.com/reaction/1094625

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantOripavineHCID 5462306—
Reactant14-HydroxymorphinoneHCID 71751419—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductOxymorphoneHCID 528460495%

Reaction Steps

A mixture of CPS-0 (6.92 g contains 76% (5.26 g, 17.7 m mol) of oripavine), meta-chloroperoxybenzoic acid (MCPBA, 4.30 g) and glacial acetic acid (52 ml) is stirred at room temperature for 5 hours. The amount of oripavine is then expected to be not more than 1% by HPLC analysis. To the resulting 14-hydroxymorphinone mixture is added 5% Pd/C (0.55 g) and hydrogenation proceeds at room temperature at 48 psig of hydrogen for about 18 hours. The amount of unreacted 14-hydroxymorphinone is expected to be not more than 0.5% by HPLC analysis. The mixture is filtered to remove the catalyst and the filtrate is evaporated to almost dryness. The residue is dissolved in water and basified to pH 9 by ammonium hydroxide. The solids are collected by filtration and dried at 90° C. and under 25-inch Hg of vacuum for 3 hours to give crude oxymorphone (approximately 95% yield expected).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134002B2
Source datasetuspto-grants-2012_03
ORD IDord-a041c4a584ba41e89f05d24670d4b59b
Source noteuspto-grants-2012_03