Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Butanal | HCID 261 | — |
| Edukt | Phosphate | HCID 1061 | — |
| Edukt | Nitrosobenzene | HCID 11473 | — |
| Edukt | L-Proline | HCID 145742 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | (R)-2-(N-Phenyl-aminooxy)-butan-1-ol | HCID 11816230 | 43% |
Reaktionsschritte
At about −20° C., L-proline (4 g, 34.8 mmol) was added to solution of n-butyraldehyde (25 mL, 278 mmol) and nitrosobenzene (15 g, 140 mmol) in acetonitrile (300 mL). The mixture was stirred at about −20° C. for about 48 hours, methanol (50 mL) and sodium borohydride (16 g, 432 mmol) were added, the mixture was stirred for about 10 minutes, and phosphate buffer was added. Following standard extractive workup with ethyl acetate, the crude product was purified by column chromatography with silica gel (petroleum ether-ethyl acetate =5:1, v:v, elution) to afford the title product (10.8 g, 43%). 1H NMR (300 MHz, CDCl3) δ 7.30-7.25 (m, 2H), 7.01-6.96 (m, 3H), 3.90-3.74 (m, 3H), 1.75-1.57 (m, 2H), 1.02 (t, J=7.8 Hz, 3H); LC-MS: m/z=182 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07767860B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-9c287d615b44465c8b90e329552ec1cf |
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| Quellennotiz | uspto-grants-2010_08 |
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