HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → 6-Methyl-5-nitropyridine-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2,6-Dimethyl-3-nitropyridine | HCID 84958 | — |
| Product | 6-Methyl-5-nitropyridine-2-carbaldehyde | HCID 3015196 | 75% |
Reaction Steps
A solution of 2,6-dimethyl-3-nitropyridine (50 g, 329 mmol) and SeO2 (5.02 g, 27.9 mmol) in dioxane (500 mL) was heated at reflux for 16 hours. The solution was filtered, the solvent removed and the residue purified by column chromatography directly (20% EtOAc/hexanes). The material was recrystalized from ethyl acetate to give 41 g of 6-methyl-5-nitropicolinaldehyde (41 g, 75%), a pale yellow solid; 1HNMR (CDCl3, 400 MHz) δ 2.94 (s, 3H), 7.98 (d, J=8.34, 1H), 8.41 (d, J=8.34, 1H), 10.09 (s, 1H). Exact mass calculated for C7H6N2O3: 166.04. found: 167.12 MS m/z (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362248B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-c7a49e4f5aea4c2ca1c8191e028b25a2 |
| Source note | uspto-grants-2013_01 |