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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530191Generated: October 27, 2026

Sodium Hydroxide → 2-Fluoro-3-(N-methylbenzamido)-N-(2-bromo-4-(heptafluoroisopropyl)phenyl)benzamide

https://huagongshe.com/reaction/530191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPerfluoroisopropyl iodideHCID 33978—
Reactant2-fluoro-3-(N-methylbenzamido)-N-(2-bromo-phenyl)benzamideHCID 117853371—
CatalystFerrous sulfate heptahydrateHCID 62662—
SolventDimethylformamideHCID 6228—
Product2-Fluoro-3-(N-methylbenzamido)-N-(2-bromo-4-(heptafluoroisopropyl)phenyl)benzamideHCID 11785338411%

Reaction Steps

0.47 g (12 mmol) of powdery sodium hydroxide and 0.54 g (1.9 mmol) of iron(II) sulfate heptahydrate were stirred in an ice bath, until the color of the mixture changed to black. Immediately after the discoloration, 3 g of N,N-dimethylformamide were added thereto, and then, a solution obtained by dissolving 0.60 g (1.4 mmol) of 2-fluoro-3-(N-methylbenzamido)-N-(2-bromo-phenyl)benzamide and 0.57 g (1.9 mmol) of heptafluoroisopropyl iodide in 3 g of N,N-dimethylformamide was added thereto, followed by stirring at room temperature for 3 hours. The obtained reaction liquid was filtered through cerite and the residue was washed with 50 mL of ethyl acetate. Then, 40 g of water were added to the resulting reaction liquid, and after performing extraction, the organic layer was dried over magnesium sulfate. Then, magnesium sulfate was filtered off, and the solvent was distilled off under reduced pressure. Thereafter, the condensed residue was purified by silica gel chromatography, to obtain 0.092 g (yield 11%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353046B2
Source datasetuspto-grants-2016_05
ORD IDord-fcca88103d4c415cb03356c757c8796c
Source noteuspto-grants-2016_05