HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178563Generated: October 29, 2026
Benzenesulfonyl chloride → HCID 67953948, compound
https://huagongshe.com/reaction/2178563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 67976467 | HCID 67976467 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67953948 | HCID 67953948 | 72.5% |
Reaction Steps
To a solution of compound 10-E (0.063 g, 0.2 mmol) in DMF (1 mL) at 0° C. was added 95% NaH (0.012 g, 0.5 mmol) and the reaction mixture was stirred for 10 minutes. Benzenesulfonyl chloride (0.053 g, 0.3 mmol) was added and the reaction mixture was stirred at room temperature overnight. The reaction was quenched by the addition of H2O and the solution was extracted with ethyl acetate. After separation of the organic and aqueous layers a sufficient amount of water was added to remove any dissolved DMF from the organic layer. The organic layer was dried over Na2SO4, filtered, and the solvent evaporated under reduced pressure to afford the crude product. The crude material was purified by flash column chromatography, eluting with a hexanes-EtOAc gradient to give compound 10-F as a white solid (0.066 g, 72%); MS m/z (M+H+) 456.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067935B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-b160a81fc8cb469bb6fa2bcc3aa6608f |
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| Source note | uspto-grants-2015_06 |
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