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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959796Generated: November 2, 2026

Dimethyl Sulfoxide → 2-Benzoxazol-2-yl-3,3-bismethylsulfanylacrylonitrile

https://huagongshe.com/reaction/1959796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium hydrideHCID 24758—
Reactant2-(1,3-Benzoxazol-2-yl)acetonitrileHCID 843325—
Product2-Benzoxazol-2-yl-3,3-bismethylsulfanylacrylonitrileHCID 1291389357%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of benzoxazol-2-ylacetonitrile (2.07 g, 13.1 mmol) dissolved in 35 mL of DMSO at room temperature under argon atmosphere was added carbon disulfide (1.10 g, 14.4 mmol) followed by iodomethane (5.20 g, 36.7 mmol). This solution was then cooled to 10° C. and sodium hydride (1.05 g, 60% by wt in oil, 26.3 mmol) was added over a period of several minutes. The solution was allowed to warm to room temperature and stirred overnight. The reaction was then quenched with an ammonium chloride solution and was extracted with 5×50 mL of ethyl acetate. The ethyl acetate was washed with brine solution (3×50 mL) and water (3×30 mL). The organic phase was dried over magnesium sulfate, filtered, and evaporated to yield a red oil. The crude material was purified by flash column chromatography eluting with CH2Cl2:MeOH=98:2 to yield 1.96 g (57%) of the desired product as a yellow oil. MS (m/z, ES+): 236.68 (M+1, 100%). The following examples illustrate the preparation of compounds disclosed in this invention.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410272B2
Source datasetuspto-grants-2013_04
ORD IDord-ac015e86f4ae4c6dad2a0327b4671c18
Source noteuspto-grants-2013_04