Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21397Erstellt: 24. Oktober 2026

Phenethyl bromide → 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)-1-phenethylpiperidine

https://huagongshe.com/de/reaction/21397

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethyl bromideHCID 7666—
EduktPotassium CarbonateHCID 11430—
Edukt3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidineHCID 13633748—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)-1-phenethylpiperidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05422358
Quelldatensatzuspto-grants-1995_06
ORD IDord-978206fb8dd144ab90f2e261895a7ce5
Quellennotizuspto-grants-1995_06