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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39326Erstellt: 24. Oktober 2026

Potassium Iodide → 6-Ketonalbuphine

https://huagongshe.com/de/reaction/39326

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt(Bromomethyl)cyclobutaneHCID 2734658—
Edukt14-Hydroxymorphine-6-oneHCID 15286253—
LösungsmittelDimethylacetamideHCID 31374—
Produkt6-KetonalbuphineHCID 4446500373,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524904B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-51eb604ae3e04854819ac25796e786bd
Quellennotizuspto-grants-2013_09