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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385609Generated: October 31, 2026

Oxycodone → (4R,4aS,12bS)-4a-hydroxy-9-methoxy-3-methyl-2,4,7a,13-tetrahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-7-one

https://huagongshe.com/reaction/1385609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxycodoneHCID 5284603—
ReactantThebaineHCID 5324289—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventAmmoniaHCID 222—
SolventFormic AcidHCID 284—
SolventHydrogen PeroxideHCID 784—
Product(4R,4aS,12bS)-4a-hydroxy-9-methoxy-3-methyl-2,4,7a,13-tetrahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-7-oneHCID 5359420—

Reaction Steps

Oxycodone may be prepared from thebaine by: dissolution of the thebaine in aqueous formic acid, oxidation treatment with 30% hydrogen peroxide (Seki, 18 Chem. Pharm. Bull. 671-676, 1970), neutralization with aqueous ammonia to yield 14-hydroxycodeinone and hydrogenation of the 14-hydroxycodeinone in acetic acid with the aid of a palladium-charcoal catalyst (Remington's Pharmaceutical Sciences 1041, 1975). Oxidation of thebaine may alternatively be performed using potassium dichromate in acetic acid (Freund et al., 94 J. Prakt. Chem. 135, 1916) or performic acid (Iljima et al., 60 Helv. Chim. Acta 2135-2137, 1977). Improved yield, however, has been reported to be obtained by oxidizing with m-chloroperbenzoic acid in an acetic acid-trifluoroacetic acid mixture (Hauser et al., 17 J. Med. Chem. 1117, 1974; See also, U.S. Pat. No. 4,795,813 to Schwartz, Col. 1, Lines 22-26). Yield may also be improved by hydrogenation of 14-hydroxycodeinone under a pressure of about 30 psi (Kraβnig et al. 329 Arch. Pharm. Pharm. Med. Chem. 325-326, 1996).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262266B1
Source datasetuspto-grants-2001_07
ORD IDord-85c67cda6ffe413080ae8486a31952ef
Source noteuspto-grants-2001_07