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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356603Generated: November 3, 2026

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

https://huagongshe.com/reaction/1356603

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

Temperature600 °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 600° C. for 2.7 hours. The mixture was cooled to approximately 250° C. and 0.99 g of 5% platinum on carbon was added and the mixture was hydrogenated at 60 psi of hydrogen and 400° 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 numberUS06586627B1
Source datasetuspto-grants-2003_07
ORD IDord-2fc63454b13a40fb8e3de4365d782d55
Source noteuspto-grants-2003_07