HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Bromo-4-fluoro-6-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Fluoro-2-nitroaniline | HCID 67769 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-4-fluoro-6-nitroaniline | HCID 292004 | 76% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 4-fluoro-2-nitroaniline (20 g, 128 mmol) in dichloromethane (600 mL) and acetic acid (200 mL) was slowly added bromine (13 mL, 256 mmol) at 0° C. The mixture was stirred at 0° C. for 1 hour and at ambient temperature for 16 hours. The mixture was concentrated and the residue partitioned between ethyl acetate and sodium bicarbonate solution. The organic phase was washed with sodium bisulphite solution and concentrated and the residue recrystallized from hexane/dichloromethane to provide the title compound (22.7 g, 76%). MS (DCI/NH3) m/z 236 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595406B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-19f03724a6ab4467976394b42ceedd76 |
| Source note | uspto-grants-2009_09 |