Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4979Erstellt: 23. Oktober 2026

2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one → 2-[(2-Chlorophenyl)phenylmethyl]-1-azabicyclo[2.2.2]octan-3-one

https://huagongshe.com/de/reaction/4979

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-oneHCID 297405—
EduktHCID 178418255HCID 178418255—
LösungsmittelTolueneHCID 1140—
Produkt2-[(2-Chlorophenyl)phenylmethyl]-1-azabicyclo[2.2.2]octan-3-oneHCID 19797478—

Reaktionsschritte

2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one (3 g) was dissolved in toluene (30 ml) and placed in a dropping funnel. Phenylmagnesium bromide was dissolved in toluene (15 ml) and stirred under nitrogen. This was cooled in an ice/water bath and the benzylidene solution was added dropwise. After 3 hrs the reaction was quenched with ammonium chloride solution and the aqueous layer extracted with dichloromethane (×4); this was combined with the original toluene layer and dried (MgSO4). The solvent was removed in vacuo and the residue purified by chromatography on silica eluting with 1:1 hexane:diethyl ether which afforded the title compound as a 2:1 mixture of its diastereoisomers:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05242930
Quelldatensatzuspto-grants-1993_09
ORD IDord-28e88db65242445cb373f341e46ba373
Quellennotizuspto-grants-1993_09