HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(2-Bromo-5-nitrophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Bromo-5-nitroaniline | HCID 82607 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-(2-Bromo-5-nitrophenyl)acetamide | HCID 21959509 | — |
Reaction Steps
Acetic anhydride (1.4 mL, 13.8 mmol) was added dropwise to a stirring solution of 2-bromo-5-nitroaniline (3 g, 13.8 mmol) in glacial acetic acid (30 mL) at 25° C. The reaction mixture was stirred at room temperature overnight, and then poured into water. The precipitate was collected via filtration, washed with water and dried under vacuum to provide N-(2-bromo-5-nitrophenyl)acetamide as an off white solid (3.6 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829204B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-239972a973c64e848793200ed60ab21a |
| Source note | uspto-grants-2014_09 |