Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 6-Methylpyridine-2-carbaldehyde oxime | HCID 135441746 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | (6-Methylpyridin-2-yl)methanamine | HCID 246721 | — |
Reaktionsschritte
To (E)-6-methylpicolinaldehyde oxime (0.635 g, 4.66 mmol)/acetic acid (267 μL, 4.66 mmol)/ethanol (10 mL) solution was added portionwise zinc dust (5.19 g, 79 mmol) over 30 min. The resulting mixture was stirred for additional 30 min. LCMS of reaction aliquot indicated reaction was completed. The zinc precipitates in reaction mixture was removed by filtration, and the filtrate was concentrated. The residue was basified to pH>12 with excess sat. KOH (˜7 mL), and stirred with Et2O (30 mL). The Et2O layer was collected, dried over Na2SO4, and concentrated. The residue was redissolved in EtOAc(15 mL), dried over Na2SO4, and concentrated. (6-Methylpyridin-2-yl)methanamine was obtained as a colorless oil (385 mg, 3.15 mmol, 67.6%). LCMS (m/z) 123.2 (MH+) 0.15 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09242996B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-ff5918e3df0d434fb1571b7256986869 |
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| Quellennotiz | uspto-grants-2016_01 |
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