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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23236Generated: October 26, 2026

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

https://huagongshe.com/reaction/23236

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 numberUS06849760B2
Source datasetuspto-grants-2005_02
ORD IDord-b0413f266656417db402d9d5293f8f55
Source noteuspto-grants-2005_02