HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 5-bromo-2-(2,2-difluoroethoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | 2,2-Difluoroethan-1-ol | HCID 136187 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-bromo-2-(2,2-difluoroethoxy)pyridine | HCID 21914342 | — |
Reaction Steps
2,2-Difluoroethanol (0.40 ml) was added dropwise to a suspension of sodium hydride (0.270 g) in dimethylformamide (5 ml) cooled in an ice-bath under argon. The mixture was stirred at room temperature for 40 minutes, then re-cooled in an ice-bath. A solution of 2,5-dibromopyridine (1 g) in dimethylformamide (5 ml) was added. The solution was then heated at 65° C. under argon for 18 h, allowed to cool and diluted with water (50 ml). The aqueous phase was extracted three times with ethyl acetate. The combined extracts were washed with water, brine, dried over magnesium sulphate, filtered and evaporated. The product was purified by column chromatography eluting with hexane to give a colourless oil (0.946 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07956084B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-038ab2017e4d432cb07e30f1f08f219f |
| Source note | uspto-grants-2011_06 |