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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356129Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 86583758, compound

https://huagongshe.com/reaction/1356129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
ReactantSulfurHCID 5362487—
ReactantPhosphorusHCID 5462309—
Reactant3-(5-Bromofuran-2-yl)-3-oxopropanenitrileHCID 13319359—
ProductHCID 86583758HCID 8658375865%

Reaction Steps

Following the method of Rudorf and Augustin (Phosphorus and Sulfur 1981, 9, 329), a solution of 3.02 g (14.1 mmol) 3-(5-bromo-furan-2-yl)-3-oxo-propionitrile in 25 ml dry DMSO was added dropwise to a stirred suspension of 1.13 g (28.3 mmol, 60% dispersion in mineral oil) sodium hydride in 25 ml DMSO under argon at room temperature. 0.85 ml (14.1 mmol) carbon disulfide was then added dropwise, with external water bath cooling, and stirring continued for 2 hour, after which 1.8 ml (28.3 mmol) methyl iodide was added dropwise, with external water bath cooling, and stirring continued for a further 16 h. The reaction mixture was then poured into 1 l ice-cold water, and the precipitate collected by filtration, washed with hexane, and dried in vacuo to afford 2.91 g (65%) 2-(5-bromo-furan-2-carbonyl)-3,3-bis-methylsulfanyl-acrylonitrile as a yellow crystalline solid. EI-MS m/e (%): 319 (M{81Br}+, 10), 317 (M{79Br}+, 10), 304 ([M{81Br}-CH3]+, 30), 302 ([M{79Br}-CH3]+, 45), 238 ([M—Br]+, 100), 223 (26), 210 (38), 195 (29), 175 (76), 173 (79), 95 (39), 38 (36).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586441B2
Source datasetuspto-grants-2003_07
ORD IDord-8cdf181173c040ee978ae717d06bea09
Source noteuspto-grants-2003_07