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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46807Erstellt: 24. Oktober 2026

(S)-[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol → Quinidinone

https://huagongshe.com/de/reaction/46807

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(S)-[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanolHCID 5953—
EduktSodiumHCID 5360545—
EduktFluoreneoneHCID 22281833—
LösungsmittelTolueneHCID 1140—
ProduktQuinidinoneHCID 84497—

Reaktionsschritte

A solution of fluorenone ketyl was prepared by mixing 9 g. of fluorenone and 6.5 g. of sodium in anhydrous toluene. To this solution was added a hot solution of 37 g. of anhydrous quinidine base in 150 ml. of anhydrous toluene. After 15 minutes at reflux, the reaction was complete. After extraction and neutralization treatments as in Example I, 36 g. of pure quinidinone (TLC) was obtained (97% of theory).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04175192
Quelldatensatzuspto-grants-1979_11
ORD IDord-2e349f16a0ab4c7baaf37321e4e4dae6
Quellennotizuspto-grants-1979_11