HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → 1-(2-BroMoethoxy)-4(trifluoroMethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(2-BroMoethoxy)-4(trifluoroMethyl)benzene | HCID 14645048 | 21.4% |
Reaction Steps
A suspension of 5.0 g of 4-hydroxybenzotrifluoride, 17.4 g of 1,2-dibromoethane and 2.6 g potassium carbonate in acetone (100 ml) was heated under reflux for 3 days. The reaction solution was diluted with water and ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated ammonium chloride (×2), dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give 1.78 g of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07544835B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-1bf3eed9062147fbb3c144a31cbaa9f9 |
| Source note | uspto-grants-2009_06 |