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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxide | HCID 961 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | (1-Imidazolyl)acetonitrile | HCID 11804695 | — |
| Reactant | 1,2-Dibromo-1-(4-t-butoxyphenyl)ethane | HCID 15233495 | — |
| Reactant | Dithiolate | HCID 86638310 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(1-Imidazolyl)-2-{4-(hydroxyphenyl)-1,3-dithiolane-2-ylidene}acetonitrile | HCID 53794773 | 16.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05391558 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-e9318161b6864b47bc285047657ab466 |
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| Source note | uspto-grants-1995_02 |
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