HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-(Benzyloxy)-1-bromo-2-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-3-methoxyphenol | HCID 347955 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(Benzyloxy)-1-bromo-2-methoxybenzene | HCID 12985923 | — |
Reaction Steps
A mixture of 4-bromo-3-methoxyphenol (21 g), benzyl bromide (13.5 ml), potassium carbonate (21.4 g) and acetone (200 ml) was stirred at room temperature for 24 h. The insoluble materials were removed by filtration and the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1) to give 4-benzyloxy-2-methoxybromobenzene (25 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726306 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-2c708472c83f40bf8ae9adf5f16de858 |
| Source note | uspto-grants-1998_03 |