HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2'-Bromoacetanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Bromoaniline | HCID 11992 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2'-Bromoacetanilide | HCID 136416 | 75% |
Reaction Steps
2-Bromo-1-acetylaminobenzene was synthesized in the usual manner from 2-bromoaniline. That is, 150 ml of acetonitrile was added to 25.0 g of 2-bromoaniline, then 15.1 ml of glacial acetic acid was added thereto, and the reaction mixture was heated under reflux for 2 hours. After bringing its temperature to room temperature, 300 ml of ethyl acetate was added thereto, and after the resulting mixture was washed with water twice, the solvent was distilled off, and recrystallization of the crude crystals from a hexane/ethyl acetate solvent mixture was carried out, to obtain 23.2 g (yield: 75%) of 2-bromo-1-acetylaminobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05006660 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-5591e418656b4c909c222813e8b51adb |
| Source note | uspto-grants-1991_04 |