HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → 2-(4-Bromoanilino)-1-phenyl-1-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Bromoanilino)-1-phenyl-1-ethanone | HCID 804442 | 80.3% |
Reaction Steps
To a solution containing 4-bromoaniline (7.42 g, 0.0431 mol) and 2-bromoacetophenone (8.58 g, 0.0431 mol) in N,N-dimethylformamide (200 mL) N,N-diisopropylethylamine was added dropwise and the reaction mixture was stirred at ambient temperature for five hours. The solvent was removed under reduced pressure and the residue partitioned between dichloromethane (150 mL) and water (100 mL). The organic phase was dried with magnesium sulfate and concentrated under reduced pressure. The residue was suspended in diethyl ether and the precipitate was collected by filtration and dried to yield 2-(4-bromoanilino)-1-phenyl-1-ethanone (10.03 g, 0.0346 mol) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921763B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-1788061007714db6be220df7c7d58e99 |
| Source note | uspto-grants-2005_07 |