HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-1-[3-(trifluoromethyl)phenyl]ethan-1-one → HCID 66939373, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-1-[3-(trifluoromethyl)phenyl]ethan-1-one | HCID 2778386 | — |
| Reactant | HCID 58127823 | HCID 58127823 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66939373 | HCID 66939373 | 92% |
Reaction Steps
To a solution of the compound (209 mg, 1.0 mmol) obtained in Example 178a in ethanol (4 mL) was added 2-bromo-1-[3-(trifluoromethyl)phenyl]ethanone (267 mg, 1.0 mmol), and the mixture was heated under reflux for 1.5 hr. The reaction mixture was concentrated under reduced pressure, the residue was diluted with diluted aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give the title compound (346 mg, 92%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461348B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-c9d75729b9444b659c374c29b82845b1 |
| Source note | uspto-grants-2013_06 |