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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 254267Erstellt: 25. Oktober 2026

Hydrochloric Acid → Oxycodone

https://huagongshe.com/reaction/254267

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthylenediaminetetraacetic AcidHCID 6049—
EduktAcetic acid, mercapto-, ion(1-)HCID 5086465—
EduktOxycodoneHCID 5284603—
EduktSodium ThioglycolateHCID 23690444—
ProduktOxycodoneHCID 5284603—
Produkt(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—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07875623B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-a040a0d05a854401972464bb2c39f036
Quellennotizuspto-grants-2011_01