Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 6-Methylpyridine-2,4-diol | HCID 54691419 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54684290 | HCID 54684290 | 60.2% |
Reaction Steps
4-Hydroxy-6-methyl-1H-pyridin-2-one (25 g, 0.2 mol) and N-chlorosuccinimide (29.4 g, 0.22 mol) were dissolved in 200 mL of acetic acid. The reaction was heated at 115° C. for 6 hours. The reaction was cooled to room temperature, the solid was filtered, and washed with acetic acid and hexanes. The solid was dried in a vacuum oven overnight to give a white solid (19.2 g, 60%): 1H NMR (300 MHz, DMSO-d6) δ 11.46 (br s, 1H), 11.04 (s, 1H), 5.79 (s, 1H), 2.09 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07629363B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-681934a651f64c239b69fdee7a8b8fa1 |
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| Source note | uspto-grants-2009_12 |
|---|