HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromoaniline → N-(4-bromophenyl)-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | 1-Bromo-2-nitrobenzene | HCID 11341 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(4-bromophenyl)-2-nitroaniline | HCID 12000290 | 22% |
Reaction Conditions
| Temperature | 180 °C |
|---|
Reaction Steps
A mixture made from 10 g (49.5 mmol) of 2-bromo nitrobenzene, 13 g (163 mmol) of sodium acetate and 10 g (59 mmol) of 4-bromo aniline was stirred with heating at the temperature of 180° C. under the atmosphere of nitrogen gas for 8 hours. The reacted solution was cooled down to room temperature, diluted with ethyl acetate and filtered. After concentrating the filtrate, and by washing the residue with methanol 3.8 g of (4-bromophenyl)-(2-nitrophenyl) amine was obtained as orange crystals (yield: 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851071B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-ac3cb601fa494f9790a5c182603fd5ed |
| Source note | uspto-grants-2010_12 |