HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356616Generated: November 2, 2026
Water → 4'-Chloro-N-ethyl-2'-nitro-p-toluenesulfonanilide
https://huagongshe.com/reaction/1356616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 3691019 | HCID 3691019 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4'-Chloro-N-ethyl-2'-nitro-p-toluenesulfonanilide | HCID 11703132 | 74% |
Reaction Steps
To a suspension of sodium hydride (60%, 0.05 g (1.25 mmol)) in DMF (2.0 ml), 4′-chloro-2′-nitro-p-toluenesulfonanilide (0.30 g (0.92 mmol)) was added with stirring at room temperature. To the resulting mixture, after 15 minutes' stirring at room temperature, ethyl iodide (0.50 ml (6.25 mmol)) was added dropwise. After one hour's heating at 100° C. with stirring, the reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with water and saturated sodium chloride solution, successively, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography with ethyl acetate-hexane (1:3) as eluent, giving 0.24 g (74%) 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-78848824f0a34be0838a771795f6138c |
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| Source note | uspto-grants-2003_07 |
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