Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | 2-(Acetylamino)-3-phenyl-2-propenoic acid | HCID 95631 | — |
| Edukt | 1,2-Bis(o-anisylphenylphosphino) ethane | HCID 15061558 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | N-Acetyl-L-phenylalanine | HCID 74839 | — |
Reaktionsschritte
A solution of 0.013 g. of [Rh(COD)Cl]2 (0.026 m moles) and 0.024 g. 1,2-bis(o-anisylphenylphosphino) ethane prepared in Example 1 (0.051 m moles) in 5 ml. of methanol was made with stirring for 15 minutes at 25° C. With careful exclusion of air, 0.5 ml. of this solution was added to a slurry of 1.00 g. of α-acetamidocinnamic acid in 25 ml. of 88% i-propanol at 50° C. and the resulting mass was subjected to 3.5 atm. (abs. pressure) of hydrogen. The hydrogenation reaction was completed in 0.7 hours. N-acetyl-L-phenylalanine can be isolated from the reaction mass by crystallization. Analysis of the reaction mixture showed that an optical purity of 92.8% of the L isomer was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04220590 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-17d0cbbf7dd445a09b6e06562cd8dd86 |
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| Quellennotiz | uspto-grants-1980_09 |
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