HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396277Generated: October 29, 2026
Water → 6-Chloro-2-hydroxy-3-nitrobenzenesulfonamide
https://huagongshe.com/reaction/396277
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,6-Dichloro-3-nitrobenzene-1-sulfonamide | HCID 11173285 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Chloro-2-hydroxy-3-nitrobenzenesulfonamide | HCID 11276817 | 77% |
Reaction Steps
A mixture of 2,6-dichloro-3-nitrobenzenesulfonamide (2.61 g, 9.64 mmol), 60% sodium hydride (1.15 g, 28.9 mmol) and water (174 μL, 9.64 mmol) was heated to 45° C. while kept at argon atmosphere for 3 days. The reaction was monitored by 1H NMR. 0.1 equivalent water was added to the mixture when the reaction was not completed. The solvent was evaporated when the reaction almost completed indicated by 1H NMR. The residue was diluted with ethyl acetate and washed with 1N aq. HCl. The solvent was concentrated to give the crude material. Column chromatography on silica gel, eluting with ethyl acetate/hexane/acetic acid (50/48/2, v/v/v), gave the desired product (1.87 g, 77%). EI-MS (m/z)250.84, 252.89 (M−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608077B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-aa8dcc0cb7e14153906f92d8bb186c5d |
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| Source note | uspto-grants-2003_08 |
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