HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-bromo-4-(trifluoromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Bromo-4-(trifluoromethyl)benzoic acid | HCID 67605 | — |
| Product | Ethyl 2-bromo-4-(trifluoromethyl)benzoate | HCID 15766264 | 100% |
Reaction Steps
238 g (0.885 mol) of 2-bromo-4-(trifluoromethyl)benzoic acid, 1000 ml of absolute ethanol and 100 ml of concentrated sulfuric acid are introduced successively into a 2-liter round-bottomed flask. The reaction mixture is brought to reflux for 6 hours and then poured, after cooling, onto 2.5 liters of ice-cold water; the oil formed is extracted with ethyl acetate. The organic phase is successively washed with water, with 1N sodium hydroxide solution and then again with water. After drying over magnesium sulfate, the solvent is evaporated to provide 263 g (yield: 100%) of ethyl 2-bromo-4-(trifluoromethyl)benzoate in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05514719 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-bb6e42ca444748fd9e19e6039f031dd1 |
| Source note | uspto-grants-1996_05 |