HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Aminoacetophenone → 1-(4-Amino-3-bromo-phenyl)-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Aminoacetophenone | HCID 7468 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(4-Amino-3-bromo-phenyl)-ethanone | HCID 1515281 | 85% |
Reaction Steps
To a solution of 4-aminoacetophenone (5.67 g, 0.0419 mol) in 30 mL of CH3CN at 0° C. was added N-bromosuccinimide (7.83 g, 0.0439 mol) in 20 mL of CH3CN dropwise. The reaction was allowed to warm to room temperature and concentrated in vacuo after stirring 16 h. The crude residue was dissolved in EtOAc (100 mL), washed with saturated aqueous NaHCO3 (1×100 mL), brine (1×100 mL) and dried (Na2SO4). The solvent was removed under vacuum to afford the title compound (7.62 g, 85%) as a yellow solid. Mass spectrum (ESI, m/z): Calcd. for C8H8BrNO, 213.9 (M+H). found 214.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221797B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-61db2ab273554d48ad38bae457ecc39e |
| Source note | uspto-grants-2015_12 |