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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Perfluoroisopropyl iodide | HCID 33978 | — |
| Reactant | 2-fluoro-3-(N-methylbenzamido)-N-(2-bromo-phenyl)benzamide | HCID 117853371 | — |
| Catalyst | Ferrous sulfate heptahydrate | HCID 62662 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Fluoro-3-(N-methylbenzamido)-N-(2-bromo-4-(heptafluoroisopropyl)phenyl)benzamide | HCID 117853384 | 11% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353046B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-fcca88103d4c415cb03356c757c8796c |
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| Source note | uspto-grants-2016_05 |
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