Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | Methyl (2S)-2-(2,3,4-trifluoroanilino)propionate | HCID 10125210 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (2S)-2-(2,3,4-Trifluoroanilino)propanol | HCID 11401466 | — |
Reaktionsschritte
At room temperature, sodium borohydride (35.7 mg) was suspended in IPE (0.2 ml). Then a solution (0.8 ml) of methyl (2S)-2-(2,3,4-trifluoroanilino)propionate (200 mg, 99.8% ee) in IPE was added to the solution. After adding methanol (137.4 mg), the liquid reaction mixture was stirred for 2 hours. Then water was added to the liquid reaction mixture followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of ammonium chloride and dried over anhydrous magnesium sulfate. After evaporating the solvent, the obtained residue was subjected to silica gel column chromatography to thereby give 176 mg (99.8% ee) of the title compound as an oily substance. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 51.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07087778B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-114c8b0cd3ee46b0b31d316ba3f13637 |
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| Quellennotiz | uspto-grants-2006_08 |
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