HuagongsheHuagongshe Chemistry Print Report · For research reference only
Selenium Dioxide → 3-Hydroxy-6-methylpyridine-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 3-Hydroxy-2-hydroxymethyl-6-methylpyridine | HCID 135128 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Hydroxy-6-methylpyridine-2-carbaldehyde | HCID 12421986 | 57.3% |
Reaction Steps
3-Hydroxy-6-methyl-2-pyridine methanol (20.0 g, 0.14 mol) and selenium dioxide(8.0 g, 72 mmol) were dissolved in 140 mL of 1,4-dioxane and 280 mL of absolute ethanol. The resulting mixture was heated at 80°-85° C. for 12 h. The selenium precipitate was removed by filtration and the filtrate was concentrated to dryness in vacuo. The dark red residue was sublimed at 90° C. and 14 mmHg for 6 h to obtain 11.0 g (56%) of pure product, m.p. 101°-102° C.; 1H NMR (CDCl3) d: 10.50 (br s, 1H), 10.03 (s, 1H), 7.27 (s, 2H); 2.53 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05714615 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-6b51a0c2361f4838a200fe41f8592ec1 |
| Source note | uspto-grants-1998_02 |