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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355907Generated: October 27, 2026

Dimethyl Sulfoxide → 2-(5-Methyl-furan-2-carbonyl)-3,3-bis-methylsulfanyl-acrylonitrile

https://huagongshe.com/reaction/1355907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
ReactantSulfurHCID 5362487—
ReactantPhosphorusHCID 5462309—
Reactant3-(5-Methylfuran-2-yl)-3-oxopropanenitrileHCID 15324060—
Product2-(5-Methyl-furan-2-carbonyl)-3,3-bis-methylsulfanyl-acrylonitrileHCID 8658375189%

Reaction Steps

Following the method of Rudorf and Augustin (Phosphorus and Sulfur 1981, 9, 329), a solution of 1.77 g (11.9 mmol) 3-(5-methyl-furan-2-yl)-3-oxo-propionitrile in 10 ml dry DMSO was added dropwise to a stirred suspension of 0.95 g (23.7 mmol, 60% dispersion in mineral oil) sodium hydride in 10 ml DMSO under argon at room temperature. 0.72 ml (11.9 mmol) carbon disulfide was then added dropwise, with external water bath cooling, and stirring continued for 1 hour, after which 1.48 ml (23.7 mmol) methyl iodide was added dropwise, with external water bath cooling, and stirring continued for a further 1 h. The reaction mixture was then poured into 300 ml ice-cold water, and the precipitate collected by filtration and dried in vacuo to afford 2.67 g (89%) 2-(5-methyl-furan-2-carbonyl)-3,3-bis-methylsulfanyl-acrylonitrile as a yellow crystalline solid. ES-MS m/e (%): 254 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586441B2
Source datasetuspto-grants-2003_07
ORD IDord-211586d5256e48c9aa8e5ecfbc6f03cb
Source noteuspto-grants-2003_07