Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363254Generated: November 1, 2026

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

https://huagongshe.com/reaction/363254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactantphenylalaninol, (S)-HCID 447213—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
Product(S)-2-benzylamino-3-phenyl-1-propanolHCID 1051426748.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872298
Source datasetuspto-grants-1999_02
ORD IDord-51fe006980d84d6f9230a21ba478aee4
Source noteuspto-grants-1999_02