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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-3-(trifluoromethoxy)anilineHCID 25210503—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-fluoro-3-(trifluoromethoxy)anilineHCID 8668280890.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212168B2
Source datasetuspto-grants-2015_12
ORD IDord-ea54609e682441489aee18255c5c80b3
Source noteuspto-grants-2015_12