HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85323Generated: October 25, 2026
Tetracyanoethylene → 2-Cyano-3-[5-[2-(4-dibutylamino-2-methoxyphenyl)vinyl]thiophene-2-yl]-2-butenedinitrile
https://huagongshe.com/reaction/85323
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetracyanoethylene | HCID 12635 | — |
| Reactant | Dibutyl[3-methoxy-4-[2-(thiophene-2-yl)vinyl]phenyl]amine | HCID 68008836 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Cyano-3-[5-[2-(4-dibutylamino-2-methoxyphenyl)vinyl]thiophene-2-yl]-2-butenedinitrile | HCID 86667605 | 41.8% |
Reaction Steps
In 7 ml of N,N-dimethylformamide, 235 mg (1.83 mmol) of tetracyanoethylene was dissolved. With stirring under ice cooling, 600 mg (1.75 mmol) of dibutyl[3-methoxy-4-[2-(thiophene-2-yl)vinyl]phenyl]amine was dissolved in 2 ml of N,N-dimethylformamide and added dropwise. The mixture was stirred for 1.5 hours. After the ice bath was removed, the mixture was stirred at room temperature for 1 hour and further stirred with heating at 50° C. overnight. After the reaction mixture was poured into 80 ml of water, extraction with chloroform, washing with a saturated saline solution, drying over anhydrous sodium sulfate, and concentration were performed. The residue was purified by silica gel column chromatography and washed with methanol to give 324 mg of a dark reddish crystal having a mp of 189-192° C. (yield: 41.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846955B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a674ceb4ec954a34a54c2ac91ef6271e |
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| Source note | uspto-grants-2014_09 |
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