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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265692Generated: October 26, 2026

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

https://huagongshe.com/reaction/265692

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%

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 numberUS05648511
Source datasetuspto-grants-1997_07
ORD IDord-9b97a430c9734f28a9cce2f9b1f67ed7
Source noteuspto-grants-1997_07