HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 2-Bromo-4-ethoxy-1-(trifluoromethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-bromo-4-(trifluoromethoxy)phenol | HCID 2757194 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Bromo-4-ethoxy-1-(trifluoromethoxy)benzene | HCID 57582332 | 125% |
Reaction Steps
To a solution of the 3-bromo-4-trifluoromethoxyphenol (1.0 g, 2.48 mmol) in acetone (30 ml) was added ethyl iodide (0.795 ml, 9.94 mmol) followed by potassium carbonate (1.37 g, 9.94 mmol) and the reaction was heated to reflux for 12 hrs. The reaction mixture was cooled then filtered and concentrated in vacuo. Dichloromethane (20 ml) and water (20 ml) were added and the solution was filtered through a phase separation cartridge. The organic layer was collected, and evaporated in vacuo to afford crude title compound as a colourless oil (884 mg, 80%). Material was taken on without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08134007B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-20340259bcdd4fb399ce84fc14ed2e5a |
| Source note | uspto-grants-2012_03 |