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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | phenylalaninol, (S)- | HCID 447213 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-2-benzylamino-3-phenyl-1-propanol | HCID 10514267 | 48.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06849760B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-b0413f266656417db402d9d5293f8f55 |
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| Source note | uspto-grants-2005_02 |
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