HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-(Benzyloxy)-6-bromonaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Cesium carbonate | HCID 10796 | — |
| Product | 2-(Benzyloxy)-6-bromonaphthalene | HCID 640595 | — |
Reaction Steps
To the commercially available 6-bromo-naphthalene-2-ol (1) (1 equi.) and benzyl bromide (2) (1 equi.) in DMF (3mL/mmole), cesium carbonate (1.25 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h, quenched with water, extracted with ethyl acetate:hexane (1:1), washed with brine, over MgSO4, and concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06703082B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-2d89c4a6c19742cea11d66a9ead29487 |
| Source note | uspto-grants-2004_03 |