HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356704Generated: October 26, 2026
Water → 4'-Chloro-4-cyano-N-ethyl-2'-nitrobenzenesulfonanilide
https://huagongshe.com/reaction/1356704
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Cyanobenzenesulfonyl chloride | HCID 39497 | — |
| Reactant | Benzenamine, 4-chloro-N-ethyl-2-nitro- | HCID 97006 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Chloro-4-cyano-N-ethyl-2'-nitrobenzenesulfonanilide | HCID 18509265 | 64.6% |
Reaction Steps
To a suspension of sodium hydride (60%, 0.10 g (2.50 mmol)) in tetrahydrofuran (THF)(3.0 ml), 4-chloro-N-ethyl-2-nitroaniline (0.40 g (1.99 mmol)) was added with stirring at room temperature. To the mixture, after stirring for 30 minutes at room temperature, 4-cyanobenzenesulfonyl chloride (0.50 g (2.48 mmol)) was added and the resulting mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into water and the resulting mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography with ethyl acetate-hexane (1:2) as eluent, to give 0.47 g (64%) of the title compound as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586617B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-ee92ba0fa7e3409690faf65a571f39f1 |
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| Source note | uspto-grants-2003_07 |
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