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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1912338Erstellt: 25. Oktober 2026

Sulfuric Acid → 10-Benzyl-3,10-diazabicyclo[4.3.1]decan-4-one

https://huagongshe.com/reaction/1912338

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktPotassium CarbonateHCID 11430—
EduktPotassium HydroxideHCID 14797—
EduktSodium AzideHCID 33557—
Edukt9-Benzyl-9-azabicyclo[3.3.1]nonan-3-oneHCID 419531—
LösungsmittelChloroformHCID 6212—
Produkt10-Benzyl-3,10-diazabicyclo[4.3.1]decan-4-oneHCID 4579274595%

Reaktionsschritte

To a solution of 9-benzyl-9-azabicyclo[3.3.1]nonan-3-one (0.5 g) in chloroform (4.4 ml), cooled down to −5° C., 1 ml of conc. H2SO4 is dropwise added while maintaining the temperature below 15° C. Then NaN3 (0.28 g) is slowly added, at small portions so to avoid temperatures in the reaction mixture higher than 35° C. The mixture is then heated at reflux for 2 hours. The reaction mixture is poured into a vessel containing about 200 ml of ice. Solid K2CO3 is added up to a strongly alkaline pH. An emulsion is formed, that is added of 25 ml of a 60% KOH aqueous solution. Stirring is effected for 10 minutes. At the end the formed inorganic salts are filtered and the reaction mixture extracted with chloroform. The organic phase is dehydrated with sodium sulphate and the solvent evaporated. 0.50 g of 10-benzyl-3,10-diazabicyclo[4.3.1]decan-4-one (1py1) are obtained as a light solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08609659B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-5b1c90349f3a475eab5c9027473a2366
Quellennotizuspto-grants-2013_12