Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl morpholine oxide | HCID 82029 | — |
| Edukt | (6-Methoxypyridin-3-yl)boronic acid | HCID 2734368 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-Hydroxy-2-methoxypyridine | HCID 11622335 | — |
Reaktionsschritte
At RT, 50 g (327 mmol) of 6-methoxypyridin-3-ylboronic acid were added to a solution of 46.0 g (392 mmol) of N-methylmorpholine N-oxide in 500 ml of dichloromethane, and the mixture was stirred at 50° C. for 14 h. Additional N-methylmorpholine N-oxide was added until the reaction had gone to completion. The reaction mixture was concentrated under reduced pressure and the crude product was purified by flash chromatography (silica gel 60, cyclohexane/ethyl acetate mixtures). Yield: 32.9 g (80% of theory)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09434690B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-873065e9d4b141dcac24f012c4cf7220 |
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| Quellennotiz | uspto-grants-2016_09 |
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