HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-Bromo-5-methylpyridine 1-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Bromo-5-methylpyridine | HCID 564216 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-5-methylpyridine 1-oxide | HCID 13178737 | 7,630.9% |
Reaction Steps
To a solution of 2-bromo-5-methylpyridine (4 g, 2.3 mmol) in dichloromethane (500 mL) was added m-CPBA (52 g, 304 mmol) at 0° C. The reaction mixture was stirred at room temperature for 20 hours and the then the pH was adjusted to about 9 with a saturated solution of K2CO3. The organic layers were separated and concentrated to give a residue which was purified by flash silica chromatography eluted with petroleum ether/ethyl acetate (1:1) to give 2-bromo-5-methylpyridine 1-oxide (33 g; 75%). 1H NMR (CDCL3): δ ppm 8.25 (s, 1H), 8.75 (d, 1H, J=8.4 Hz), 6.95-6.94 (m, 1H), 2.30 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073918B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-7d3dfce78ee345d4b93013e086bf4d51 |
| Source note | uspto-grants-2015_07 |