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
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% |
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 | US05648511 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-9b97a430c9734f28a9cce2f9b1f67ed7 |
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| Source note | uspto-grants-1997_07 |
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