HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504332Generated: October 30, 2026
N-bromobutanimide → 4-Bromo-2-fluoro-3-(trifluoromethoxy)aniline
https://huagongshe.com/reaction/1504332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Fluoro-3-(trifluoromethoxy)aniline | HCID 25210503 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-2-fluoro-3-(trifluoromethoxy)aniline | HCID 86682808 | 90.3% |
Reaction Steps
To a solution of 2-fluoro-3-(trifluoromethoxy)aniline (1.0 g, 5.13 mmol) dissolved in DMF (2 mL) at 0° C. was slowly added a solution of cold N-bromosuccinimide (0.91 g, 5.13 mmol) dissolved in DMF (6 mL) over 5 min. The reaction mixture was stirred at 0° C. for 1 h, extracted with EtOAc (125 mL) and washed with water (3×25 mL). The combined aqueous layers were extracted with EtOAc (75 mL). The combined organic layers were washed with brine (25 mL), dried over sodium sulfate, filtered, and concentrated to produce the title compound as a dark colored liquid (1.27 g, 90% yield). (m/z): [M+H]+ calcd for C7H4BrF4NO 273.94. found 273.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09212168B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-ea54609e682441489aee18255c5c80b3 |
|---|
| Source note | uspto-grants-2015_12 |
|---|