HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one → 2-[(2-Chlorophenyl)phenylmethyl]-1-azabicyclo[2.2.2]octan-3-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one | HCID 297405 | — |
| Edukt | HCID 178418255 | HCID 178418255 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-[(2-Chlorophenyl)phenylmethyl]-1-azabicyclo[2.2.2]octan-3-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05242930 |
| Quelldatensatz | uspto-grants-1993_09 |
| ORD ID | ord-28e88db65242445cb373f341e46ba373 |
| Quellennotiz | uspto-grants-1993_09 |