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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21386Erstellt: 24. Oktober 2026

Phenethyl bromide → 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)-1-phenethylpiperidine

https://huagongshe.com/de/reaction/21386

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethyl bromideHCID 7666—
EduktPotassium CarbonateHCID 11430—
Edukt3-(R)-(1-cyano-1,1-diphenylmethyl)-piperidineHCID 22853758—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)-1-phenethylpiperidineHCID 22853756—

Reaktionsschritte

A mixture containing 3-(R)-(+)-(1-cyano-1,1-diphenylmethyl)piperidine (1 g), phenethyl bromide (0.-67 g), anhydrous potassium carbonate (1.5 g) and acetonitrile (25 ml) was heated under reflux for 4 hours. The mixture was partitioned between dichloromethane (50 ml) and 10% aqueous potassium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (3×30 ml)--. The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with hexane containing dichloromethane (30% up to 70%) then dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from acetonitrile to give the title compound as colourless rhombs, yield 0.72 g, m.p. 134°-138° C., [α]D25 +13.3° (C 1.0, CH2Cl2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05422358
Quelldatensatzuspto-grants-1995_06
ORD IDord-19fb6cb68a014b86af7f9d7ebbf543ed
Quellennotizuspto-grants-1995_06