HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-Bromo-5-chloro-3-methoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromo-5-chloropyridin-3-ol | HCID 14740053 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-5-chloro-3-methoxypyridine | HCID 19081434 | — |
Reaction Steps
To a DMF (60 mL) solution containing 2-bromo-5-chloro-3-hydroxypyridine (19.95 g, 95.7 mmol) at 0° C. was added NaH (2.53 g, 105.3 mmol) portion wise. After the cessation of H2 evolution, CH3I (14.26 g, 100.5 mmol) was added dropwise and the reaction stirred ~16 h. Water (1.9 mL) was added and the solvent removed under reduced pressure. The concentrate was triturated with 5 portions of CH2Cl2. The combined organic phases were washed with sat. NaCl solution, dried with K2CO3, filtered, and concentrated in vacuo. Silica gel chromatography (95:5 Hexane:EtOAc) of the concentrate afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763444 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-02d974ba0a9744c0992196be9d522c6f |
| Source note | uspto-grants-1998_06 |