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
Dissolve 0.3 mol of 1-(2,4,6-trimethylphenyl)-1-ethanone in 200 ml of glacial acetic acid, and add 31.8 g of bromine dropwise while maintaining the reaction medium at a temperature below 10° C. When the addition is complete, allow the reaction medium to return to room temperature and leave at this temperature for 2 hours. Then pour the reaction medium into 500 ml of ice-cold water and extract the aqueous phase with ethyl ether. Wash the organic extracts with saturated aqueous sodium bicarbonate solution and then with salt water, and dry over anhydrous magnesium sulphate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464847 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-1d73ba4322e04fd2a72493a5e232af53 |
| Source note | uspto-grants-1995_11 |