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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274856Generated: October 31, 2026

Hydroxide → 2-(1-Imidazolyl)-2-{4-(hydroxyphenyl)-1,3-dithiolane-2-ylidene}acetonitrile

https://huagongshe.com/reaction/274856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxideHCID 961—
ReactantCarbon DisulfideHCID 6348—
Reactant(1-Imidazolyl)acetonitrileHCID 11804695—
Reactant1,2-Dibromo-1-(4-t-butoxyphenyl)ethaneHCID 15233495—
ReactantDithiolateHCID 86638310—
SolventDimethyl SulfoxideHCID 679—
Product2-(1-Imidazolyl)-2-{4-(hydroxyphenyl)-1,3-dithiolane-2-ylidene}acetonitrileHCID 5379477316.8%

Reaction Steps

In 40 ml of dimethyl sulfoxide were dissolved 4.6 g (0.004 mol) of 1-cyanomethylimidazole, 3.1 g (0.005 mol) of carbon disulfide and 5.2 g of pottassium hydroxide powder by stirring at room temperature for 1 hour to prepare a dithiolate solution. The solution was added dropwise to a solution of 14.8 g (0.04 mol) of 1,2-dibromo-1-(4-t-butoxyphenyl)ethane in 40 ml of dimethyl sulfoxide at 30° C., followed by stirring for 2 hours. To the reaction mixture was added 200 ml of icewater, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate, and concentrated to obtain a mixture of geometric isomers as a viscous oily substance. Purification of the product by silica gel chromatography gave 2.4 g (yield: 16.8%) of a Z-isomer and 4.5 g (yield: 31.5%) of an E-isomer both as a viscous oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391558
Source datasetuspto-grants-1995_02
ORD IDord-e9318161b6864b47bc285047657ab466
Source noteuspto-grants-1995_02