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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1813891Generated: November 3, 2026

Dimethyl Sulfoxide → HCID 2819125, compound

https://huagongshe.com/reaction/1813891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
Reactant2-(4-Chlorobenzenesulfonyl)acetonitrileHCID 735829—
SolventWaterHCID 962—
ProductHCID 2819125HCID 281912565%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(4-chlorobenzenesulfonyl) acetonitrile (600 mg, 2.78 mmol) in anhydrous DMSO (8 ml) under an argon atmosphere was added carbon disulfide (212 mg, 2.78 mmol). The reaction mixture was cooled to approximately 0° C. and 2 equivalents of sodium hydride (5.56 mmol) was added in one portion. The resulting thick reaction mixture was swirled until homogeneous and allowed to warm to room temperature for one hour with stirring. The reaction mixture was cooled again to 0° C. and 2 equivalents of iodomethane (5.56 mmol) was added under argon. The reaction mixture was allowed to gradually warm to room temperature and after 18 hours deionized water was added (30 ml) and the resulting slurry was stirred for 15 minutes. The solid was collected by filtration, washed with deionized water, and dried. The crude solid product thus obtained was dissolved in 25% hexanes/chloroform and purified via flash chromatography. The resulting solution was concentrated in vacuo to provide the titled compound as a light yellow solid in 65% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875771B2
Source datasetuspto-grants-2005_04
ORD IDord-da357642945e482d9ff355792910caef
Source noteuspto-grants-2005_04