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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916857Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 67953961, compound

https://huagongshe.com/reaction/1916857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantHCID 90090789HCID 90090789—
SolventDimethylformamideHCID 6228—
ProductHCID 67953961HCID 67953961—

Reaction Steps

To a solution of compound 9-C (0.100 g, 0.300 mmol) in DMF (5 mL) at room temperature was added 60% NaH (0.012 g, 0.300 mmol) and the reaction mixture was stirred for 10 minutes. Benzenesulfonyl chloride (0.053 g, 0.300 mmol) was added and the reaction mixture was stirred at room temperature overnight. DMF was removed in vacuo and water and methylene chloride were added. The organic layer was washed with H2O (2×), brine, 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 (SiO2) eluting with a gradient of 0-100% ethyl acetate in hexane to afford compound 9-D (0.040 g, 28%); MS m/z (M+H+) 476.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618150B2
Source datasetuspto-grants-2013_12
ORD IDord-5bedaaa55bf846a391692beadb8b1d84
Source noteuspto-grants-2013_12