HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356624Generated: October 27, 2026
Water → 2',4'-Dinitro-N-methylbenzenesulfonanilide
https://huagongshe.com/reaction/1356624
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-methyl-2,4-dinitroaniline | HCID 74891 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2',4'-Dinitro-N-methylbenzenesulfonanilide | HCID 18509331 | 78% |
Reaction Steps
To a suspension of sodium hydride (60%, 0.12 g (3.00 mmol)) in DMF (4.0 ml), N-methyl-2,4-dinitroaniline (0.39 g (1.98 mmol)) was added with stirring at room temperature. To the resulting mixture, after 15 minutes' stirring at room temperature, benzenesulfonyl chloride (0.38 ml (2.98 mmol)) was added dropwise. After two hours' stirring at room temperature, the reaction mixture was poured into water and extracted with diethyl ether. 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 chromatography with ethyl acetate-hexane (1:2) as eluent, to give 0.52 g (78%) 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-e66ca04d1c664206b5e1227dfb9e6c91 |
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| Source note | uspto-grants-2003_07 |
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