HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phenethyl bromide → 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)-1-phenethylpiperidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phenethyl bromide | HCID 7666 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidine | HCID 13633748 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)-1-phenethylpiperidine | HCID 21224093 | — |
Reaktionsschritte
A mixture containing 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidine (0.3 g), phenethyl bromide (0.2 g), anhydrous potassium carbonate (0.3 g) and acetonitrile (10 ml) was heated under reflux for 7 hours. The mixture was partitioned between dichloromethane (30 ml) and 10% aqueous sodium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (2×30 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a colourless solid which was recrystallised from aqueous ethanol to give the title compound, yield, 0.17 g, m.p. 175°-1780° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05422358 |
| Quelldatensatz | uspto-grants-1995_06 |
| ORD ID | ord-978206fb8dd144ab90f2e261895a7ce5 |
| Quellennotiz | uspto-grants-1995_06 |