Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2-Methyl-2-butene | HCID 10553 | — |
| Edukt | 4-Iodo-2-methoxynicotinaldehyde | HCID 10038381 | — |
| Edukt | Sodium Chlorite | HCID 23668197 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | 4-Iodo-2-methoxypyridine-3-carboxylic acid | HCID 18439940 | — |
Reaktionsschritte
To a solution of 4-iodo-2-methoxynicotinaldehyde (1 g, 3.58 mmol) in t-BuOH (6 mL), cooled at 25° C., is added 2-methyl-2-butene (6 mL, 2 M solution), Na2HPO4 (1.2 g) and water (3 mL). The reaction mixture is stirred for 5 minutes and sodium chlorite (800 mg, 8.9 mmol) is added slowly. Stirring of the mixture is continued until the aldehyde is completely consumed (3 hours, monitored by LCMS). The reaction is quenched with aq. formic acid. The mixture is partitioned between ethyl acetate (100 mL) and the organic extracts are washed with brine, dried over Na2SO4, filtered and concentrated. The white powder was used for the next reaction without any further purification. 1H NMR 400 MHz (DMSO-d6) δ 10.06 (s, 1H), 7.89 (d, 1H, J=5.6 Hz), 7.48 (d, 1H, J=5.6 Hz), 3.87 (s, 1H); MS m/z 294.1 (M+1). MS m/z 280.01 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08546370B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-9a313dd65a38467894278503abdde5f1 |
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| Quellennotiz | uspto-grants-2013_10 |
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