HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(3-bromo-5-nitrophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | ar-Bromo-ar-nitrobenzenamine | HCID 44535 | — |
| Product | N-(3-bromo-5-nitrophenyl)acetamide | HCID 10658908 | 78% |
Reaction Steps
Acetic anhydride (14 ml) was added dropwise at 0° C. to 3-bromo-5-nitroaniline (14 g, 64.5 mmol). The mixture was stirred for 30 min at RT and then quenched by the addition of crushed ice. The precipitate formed was filtered and washed with cold water to obtain off-white solid. The solid was dried under vacuum to give the product in 78% yield (13 g). 1H NMR (300 MHz, DMSO-d6): δ 10.54 (br s, 1H), 8.45 (s, 1H), 8.2 (s, 1H), 8.03 (s, 1H), 2.11 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447091B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-e6da30ffaba741e1ab8521151fa9e3e7 |
| Source note | uspto-grants-2016_09 |