Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Methylpyrimidine | HCID 18922 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Pyrimidinecarboxylic acid | HCID 169306 | — |
Reaction Steps
4-Methylpyrimidine (1.00 g, 10.6 mmol) was diluted in water (90 mL). Potassium permanganate (4.20 g, 26.5 mmol) and potassium hydroxide (4.20 g, 74.8 mmol) were added, and the mixture was heated at 75° C. for 1.5 h. Ethanol was added dropwise, and the precipitate was removed by filtration through Celite. The filtrate was concentrated under reduced pressure, diluted in water, and treated with a concentrated HCl solution until acidic. The title compound precipitated as a fine powder, which was collected by vacuum filtration and dried in a vacuum oven (770 mg, 58%): 1H NMR (DMSO-d6) δ: 13.92 (1H, br s), 9.35 (1H, d), 9.05 (1H, d), 7.99 (1H, dd).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466283B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-493d4a8103e64f5db7293fad8bb6ce4c |
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| Source note | uspto-grants-2013_06 |
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