HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromophenol → 1-(Benzyloxy)-2-bromobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(Benzyloxy)-2-bromobenzene | HCID 561828 | 40% |
Reaction Steps
2-Bromophenol (50.0 g, 0.289 mol) was dissolved in acetone (400 ml), anhydrous potassium carbonate (79.89 g, 0.578 mmol) and benzyl bromide (59.32 g, 0.347 mol) were successively added thereto and the mixture was heated to reflux for 3 hours. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane:AcOEt=95:5) to give the title compound (30.0 g, 0.114 mol, 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122543B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-dcd8325e76324bcb9357e7ce3069bc23 |
| Source note | uspto-grants-2006_10 |