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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254267생성일: 2026년 10월 26일

Hydrochloric Acid → Oxycodone

https://huagongshe.com/reaction/254267

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethylenediaminetetraacetic AcidHCID 6049—
반응물Acetic acid, mercapto-, ion(1-)HCID 5086465—
반응물OxycodoneHCID 5284603—
반응물Sodium ThioglycolateHCID 23690444—
생성물OxycodoneHCID 5284603—
생성물(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—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875623B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-a040a0d05a854401972464bb2c39f036
출처 메모uspto-grants-2011_01