돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 574357생성일: 2026년 10월 25일

Hydrochloric Acid → Oxycodone

https://huagongshe.com/reaction/574357

반응식

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 번호US09034893B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-51307fa2903d449a895c45bf80e8d3fb
출처 메모uspto-grants-2015_05