HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanone, 1-(2,4,6-trimethylphenyl)- → 2-Bromo-1-mesitylethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanone, 1-(2,4,6-trimethylphenyl)- | HCID 15461 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Bromo-1-mesitylethanone | HCID 219480 | — |
Reaction Steps
0.3 mol of 1-(2,4,6-trimethylphenyl)-1-ethanone are dissolved in 200 mi of glacial acetic acid and 31.8 g of bromine are added dropwise, while maintaining the reaction medium at a temperature below 10° C. After the addition, the reaction medium is allowed to return to room temperature and is left at this temperature for 2 hours. The reaction medium is then poured into 500 ml of ice-water and the aqueous phase is extracted with ethyl ether. The organic extracts are washed with saturated aqueous sodium bicarbonate solution end then with salted water, end are dried over anhydrous magnesium sulphate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05602132 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-26eddd4c8b874c3e8ae8c1f0383ab1fd |
| Source note | uspto-grants-1997_02 |