HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-Methoxy-4-phenoxybromobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-phenoxyphenol | HCID 18925771 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Methoxy-4-phenoxybromobenzene | HCID 18925772 | 92.1% |
Reaction Steps
To a solution of 2-bromo-5-phenoxyphenol (0.38 g, 1.4 mmol) in 6 ml acetone was added K2CO3 (0.58 g, 4.2 mmol) and iodomethane (0.26 ml, 4.2 mmol). The-reaction mixture was heated to reflux for 8 h, cooled to ambient temperature and filtered. The solvent was removed under reduced pressure and the residue was taken up in EtOAc. The organic phase was washed with 1N NaOH, water and brine. Drying over Na2SO4 afforded 0.36 g (92%) of 2-methoxy-4-phenoxybromobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05747540 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-5df851b9137742cdb02a7035877fd118 |
| Source note | uspto-grants-1998_05 |