Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1608794Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → 2-Benzyl-2-azabicyclo[2.2.2]octane-3,6-dione

https://huagongshe.com/reaction/1608794

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt2-Benzyl-2-azabicyclo[2.2.2]octan-3-oneHCID 13265545—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Benzyl-2-azabicyclo[2.2.2]octane-3,6-dioneHCID 2008569792%

Reaktionsschritte

A solution of dimethyl sulphoxide (2.34 g) in dichloromethane (5 ml) was added to a cooled (-60° C.) solution of oxalyl chloride (1.78 g) in dichloromethane (5 ml) and after 2 minutes the mixture was treated with a solution of 2-benzyl-2-azabicyclo[2.2.2]octan-3-one (2.31 g--commercially available) in dichloromethane (10 ml), stirred at -60° C. for 30 minutes, treated with triethylamine (5.05 g), allowed to warm up to room temperature, quenched with water and extracted into dichloromethane. The dichloromethane extracts were dried over sodium sulphate and evaporated. The residue was purified by chromatography on silica using hexane plus 50% ethyl acetate as eluant. Appropriate fractions were combined and evaporated to give the desired compound (2.10 g, 92%) as a colourless oil which was used directly in Preparation 3 without characterisation or further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05397800
Quelldatensatzuspto-grants-1995_03
ORD IDord-229e77b4d28c4549919d4e8d8f4e776e
Quellennotizuspto-grants-1995_03