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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254267Generated: October 25, 2026

Hydrochloric Acid → Oxycodone

https://huagongshe.com/reaction/254267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylenediaminetetraacetic AcidHCID 6049—
ReactantAcetic acid, mercapto-, ion(1-)HCID 5086465—
ReactantOxycodoneHCID 5284603—
ReactantSodium ThioglycolateHCID 23690444—
ProductOxycodoneHCID 5284603—
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

An oxycodone sample containing more than 300 ppm of 14-hydroxycodeinone was dissolved in water at pH 6.0 to produce a 7.5% solution (75 mg/mL) using 4 M HCl to effect neutralization and dissolution of the oxycodone to pH 6. Sufficient solid EDTA and solid sodium thioglycolate were added to bring the concentrations of these components in the reaction mixture to 2 mM EDTA and 20 mM thioglycolate. The pH was maintained at pH 6.0, at room temperature for 2.8 hours, after which time the reaction mixture was raised to pH 9 to precipitate the oxycodone from the solution containing the thioglycolate-Michael adduct, and excess thioglycolate. The precipitated oxycodone was washed with pH 9, 0.05 M sodium bicarbonate buffer, and dissolved in ethyl acetate. The ethyl acetate solution of oxycodone was extracted with pH 9.0, 0.05 M sodium bicarbonate buffer, and the ethyl acetate removed under reduced pressure to yield oxycodone containing less than 10 ppm of 14-hydroxycodeinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875623B2
Source datasetuspto-grants-2011_01
ORD IDord-a040a0d05a854401972464bb2c39f036
Source noteuspto-grants-2011_01