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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11241Erstellt: 23. Oktober 2026

Benzaldehyde → (S)-2-benzylamino-3-phenyl-1-propanol

https://huagongshe.com/de/reaction/11241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
Eduktphenylalaninol, (S)-HCID 447213—
EduktHCID 178418361HCID 178418361—
KatalysatorPlatinumHCID 23939—
LösungsmittelEthanolHCID 702—
Produkt(S)-2-benzylamino-3-phenyl-1-propanolHCID 1051426748,1%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

L-Phenylalaninol (5 g, 33 mmoles) and 3.59 g (33.83 mmoles) of benzaldehyde were dissolved in 55 mL of 3A ethanol under inert atmosphere in a Parr shaker and the mixture was warmed to 60° C. for 2.7 hours. The mixture was cooled to approximately 25° C. and 0.99 g of 5% platinum on carbon was added and the mixture was hydrogenated at 60 psi of hydrogen and 40° C. for 10 hours. The catalyst was filtered off, the product was concentrated under reduced pressure and the crude solid product was recrystallized from 150 mL of heptane to give 3.83 g (48% yield) of N-benzyl-L-phenylalaninol as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098202B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-44a383223fe44b849e78edd1e0e8a2be
Quellennotizuspto-grants-2006_08