HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-Bromo-3-methoxy-6-methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-6-methylpyridin-3-ol | HCID 11959101 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Bromo-3-methoxy-6-methylpyridine | HCID 10965563 | 88.3% |
Reaction Steps
A stirred mixture of 2-bromo-3-hydroxy-6-methyl-pyridine (7.89 g, 42.0 mmol), potassium carbonate (11.60 g, 83.9 mmol) and iodomethane (8.93 g, 62.9 mmol, 3.92 mL) in acetone (100 mL) was heated under reflux overnight. The mixture was filtered, evaporated and purified on silica gel (hexane:ethyl acetate, 95:5 to 9:1) to give the desired product as a white solid (7.49 g, 88.3%). 1H NMR (500 MHz, CDCl3): δ 2.46 (s, 3 H), 3.87 (s, 3 H), 7.04 (s, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06974826B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-58635002450b4ed6aaeee81ac6a86c27 |
| Source note | uspto-grants-2005_12 |