HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 4-Bromo-2,6-difluoro-1-(benzyloxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2,6-difluorophenol | HCID 2736292 | — |
| Product | 4-Bromo-2,6-difluoro-1-(benzyloxy)benzene | HCID 14207641 | — |
Reaction Steps
A stirred mixture of 4-bromo-2,6-difluorophenol (36 g, 0.172 mole), benzylchloride (21.77 g, 0.172 mole), and potassium carbonate (25 g, 0.18 mole) in demethylformamide (300 ml) was heated at 80°-90° for four hours. After cooling, the solvent was evaporated and ether added to the residue. The insoluble inorganic salts were removed by filtration, and solvent evaporated from the filtrate. The oily residue was subjected to bulb-to-bulb vacuum distillation on Kugelrohr apparatus to give the desired product as a nearly colorless oil (41 g, 80 percent): R.I.=1.5602 @25° C.; NMR (CDCl3) was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04888050 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-5f6f1a4f9b904e84b71428c8456e32ba |
| Source note | uspto-grants-1989_12 |