Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Bromo-6-methylpyridin-3-ol | HCID 11959101 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 2-Bromo-3-methoxy-6-methylpyridine | HCID 10965563 | 36,3% |
Reaktionsschritte
To the 2-bromo-6-methyl-pyridin-3-ol (I-2) 6.0 g, 31.91 mmol) and K2CO3 (8.82 g, 63.82 mmol) in acetone (100 mL) was added MeI (6.79 g, 479.87 mmol). The reaction was stirred at 45° C. under N2 for 20 h. The reaction was cooled to room temperature, filtered and concentrated. The residue was purified by silica gel column chromatography using 1:1 dichloromethane-hexanes as eluent to afford 2.34 g (36%) of 2-bromo-3-methoxy-6-methyl-pyridine (I-3, X═Br, Y═R1═CH3) as off-white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08791267B2 |
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| Quelldatensatz | uspto-grants-2014_07 |
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| ORD ID | ord-11dfd57394af4948b2968b56ecd9742d |
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| Quellennotiz | uspto-grants-2014_07 |
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