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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530190Generated: October 26, 2026

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

https://huagongshe.com/reaction/530190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPerfluoroisopropyl iodideHCID 33978—
Reactant2-fluoro-3-(N-methylbenzamido)-N-(2-methyl-phenyl)benzamideHCID 117853284—
CatalystFerrous sulfate heptahydrateHCID 62662—
SolventDimethylformamideHCID 6228—
Product2-Fluoro-3-(N-methylbenzamido)-N-(2-methyl-4-(heptafluoroisopropyl)phenyl)benzamideHCID 11785334430%

Reaction Steps

0.55 g (14 mmol) of powdery sodium hydroxide and 0.64 g (2.3 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 (1.7 mmol) of 2-fluoro-3-(N-methylbenzamido)-N-(2-methyl-phenyl)benzamide and 0.68 (2.3 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 0.26 g (yield 30%) 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-7c6cf66370de4f1a9bbc39de6bcf22e7
Source noteuspto-grants-2016_05