HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 6-Bromo-2-(bromomethyl)-3-fluoropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | (6-Bromo-3-fluoropyridin-2-yl)methanol | HCID 53485567 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Bromo-2-(bromomethyl)-3-fluoropyridine | HCID 86642285 | 95.8% |
Reaction Steps
To a stirred solution thionyl bromide (2.44 g, 11.78 mmol, 1.05 eq.) in 50 ml dry DCM, cooled to 5° C., was added dropwise a solution of (6-bromo-3-fluoropyridin-2-yl)methanol (2.54 g, 11.22 mmol, 1 eq.) and pyridine (0.931 g, 11.78 mmol, 1.05 eq.) in 15 ml dry DCM. On complete addition, the cooling bath was removed, the reaction warmed to room temperature and stirred 1.5 hr. 150 ml of water and 150 ml of DCM were added and stirring allowed for 2 mins. The organic layer was separated, dried of MgSO4 and concentrated. The residue was purified by chromatography on silica gel to give 6-bromo-2-(bromomethyl)-3-fluoropyridine (2.89 g, 87% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466176B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-b3399bd5cf3e406985a575a82f1604e6 |
| Source note | uspto-grants-2013_06 |