Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | phenylalaninol, (S)- | HCID 447213 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Platinum | HCID 23939 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | (S)-2-benzylamino-3-phenyl-1-propanol | HCID 10514267 | 48,1% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07098202B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-44a383223fe44b849e78edd1e0e8a2be |
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| Quellennotiz | uspto-grants-2006_08 |
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