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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916860Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 67953948, compound

https://huagongshe.com/reaction/1916860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantHCID 67976467HCID 67976467—
SolventDimethylformamideHCID 6228—
ProductHCID 67953948HCID 6795394872.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618150B2
Source datasetuspto-grants-2013_12
ORD IDord-c0652215de94465f875977a1b0685bd6
Source noteuspto-grants-2013_12