HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178571Generated: October 29, 2026
Benzenesulfonyl chloride → HCID 67953998, compound
https://huagongshe.com/reaction/2178571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 67966899 | HCID 67966899 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67953998 | HCID 67953998 | — |
Reaction Steps
To a solution of compound 13-C (0.450 g, 1.37 mmol) in DMF (7.5 mL) at room temperature was added 95% NaH (0.086 g, 3.42 mmol) and the reaction mixture was stirred for 10 minutes. Benzenesulfonyl chloride (0.362 g, 2.05 mmol) dissolved in DMF (2.5 mL) 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 13-D (0.552 g, 86%); MS m/z (M+H+) 470.
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-7e44040e12014d6d8db9681274f6d133 |
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| Source note | uspto-grants-2015_06 |
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