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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727383Generated: October 25, 2026

Dimethyl Sulfoxide → 3,3-Bis-methylthio-2-(2,5-dimethylbenzoyl)-acrylonitrile

https://huagongshe.com/reaction/727383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
Reactant2,5-DimethylbenzoylacetonitrileHCID 15895264—
SolventWaterHCID 962—
Product3,3-Bis-methylthio-2-(2,5-dimethylbenzoyl)-acrylonitrileHCID 15895265—

Reaction Conditions

Temperature18 °C

Reaction Steps

A solution of 4.96 g (28.6 mmol) of 2-cyano-2',5'-dimethylacetophenone in 120 mL of dry dimethyl sulfoxide and 3.43 mL (57.3 mmol) of carbon disulfide in a flame-dried 3-neck round bottom flask under dry nitrogen was stirred at 15°-18° C. while 1.41 g (58.7 mmol) of oil free sodium hydride was added in 5 portions. The resulting deep red solution was stirred for 1 hour at 18° C. and then cooled to 15° C. whereupon 3.92 mL (8.95 g, 63.0 mmol) of methyl iodide was added dropwise. The temperature rose to about 22° C. during the addition. After stirring for 2 hours at room temperature, the reaction mixture was poured into cold water and the aqueous layer was extracted three times with ethyl acetate. The combined extracts were washed three times with water and then dried with brine and magnesium sulfate. Evaporation gave 8.96 g of the title compound as a heavy orange oil which crystallized in the refrigerator. The analytical sample crystallized from ethanol, m.p. 74.5°-75.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712303
Source datasetuspto-grants-1998_01
ORD IDord-5fc6bd0138274b4e9a4829d7b07e6fe0
Source noteuspto-grants-1998_01