HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-Benzyloxy-4-bromo-2,5-difluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Bromo-2,5-difluorophenol | HCID 7018042 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyloxy-4-bromo-2,5-difluorobenzene | HCID 58086160 | — |
Reaction Steps
4-bromo-2,5-difluorophenol (2 g, 9.57 mmol) was dissolved in DMF (19 mL) and to this was added Cs2CO3 (4.37 g, 13.34 mmol) and the solution was stirred for 15 minutes before benzyl bromide (1.64 g, 9.57 mmol) was added. After 1 hour at room temperature the mixture was partitioned between ethyl acetate (100 mL)/water (100 mL), the layers were separated and the aqueous extracted with ethyl acetate. The combined organics were washed with saturated NH4Cl (100 mL), water (100 mL) and brine (2×100 mL) and dried over MgSO4. The crude material (2.74 g) was filtered through a pad of silica and eluted with 20% Et2O in hexane to afford 4-bromo-2,5-difluorophenyl phenylmethyl ether after evaporation of the solvent (2.51 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07956083B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-f30b820de2864320a822d1a79833b6db |
| Source note | uspto-grants-2011_06 |