HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(3-Bromophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-Bromophenyl)acetamide | HCID 12123 | 96% |
Reaction Steps
To a dichloromethane solution (15 ml) of 3-bromoaniline (1 g), acetic anhydride (659 μl) was added, followed by stirring at room temperature for 14 hours. This was washed with water (20 ml), and the organic layer was dried over sodium sulfate. After filtering off the sodium sulfate, the solvent was distilled off under reduced pressure. This was purified by silica gel column chromatography (dichloromethane/methanol=200/1), to obtain the desired compound (1.19 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022205B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-f1015a6ec1d24e488681d992bc221da4 |
| Source note | uspto-grants-2011_09 |