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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39326생성일: 2026년 10월 25일

Potassium Iodide → 6-Ketonalbuphine

https://huagongshe.com/reaction/39326

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물(Bromomethyl)cyclobutaneHCID 2734658—
반응물14-Hydroxymorphine-6-oneHCID 15286253—
용매DimethylacetamideHCID 31374—
생성물6-KetonalbuphineHCID 4446500373.2%

반응 단계

Noroxymorphone (1.59 g, 5.5 mmol), potassium carbonate (0.61 g, 6.1 mmol), potassium iodide (0.46 g, 2.8 mmol), and dimethyl acetamide (10 mL) were added into a round bottom flask. Bromomethylcyclobutane (0.82 g, 5.5 mmol, 0.62 mL) was added. The reaction was stirred for 7 days at room temperature. At that time, bromomethylcyclobutane (0.82 g, 5.5 mmol, 0.62 mL) was added. The reaction was stirred for an additional 7 days. HPLC analysis indicated that the noroxymorphone was consumed. Distilled water (50 mL) was added and stirred at room temperature for 6 hours. An off-white precipitate formed, which was removed by filtration. The solid was washed with distilled water (25 mL), then slurried for 24 hours in acetonitrile (25 mL). Filtration, washing the solid with acetonitrile (10 mL), and drying at room temperature under vacuum for 24 hours yielded N-(cyclobutylmethyl)-noroxymorphone (1.43 g, 73% yield) as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524904B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-51eb604ae3e04854819ac25796e786bd
출처 메모uspto-grants-2013_09