HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85320Generated: October 25, 2026
Water → 2-[5-[2-(2-Benzyloxy-4-dibutylaminophenyl)vinyl]thiophene-2-yl]-3-cyano-2-butenedinitrile
https://huagongshe.com/reaction/85320
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Tetracyanoethylene | HCID 12635 | — |
| Reactant | [3-Benzyloxy-4-[2-(thiophene-2-yl)vinyl]phenyl]dibutylamine | HCID 68008929 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[5-[2-(2-Benzyloxy-4-dibutylaminophenyl)vinyl]thiophene-2-yl]-3-cyano-2-butenedinitrile | HCID 86667604 | 31.7% |
Reaction Steps
In 3 ml of N,N-dimethylformamide, 0.13 g (1.01 mmol) of tetracyanoethylene was dissolved. With stirring under ice cooling, 0.4 g (0.95 mmol) of [3-benzyloxy-4-[2-(thiophene-2-yl)vinyl]phenyl]dibutyl amine was dissolved in 1 ml of N,N-dimethylformamide and added dropwise. The mixture was stirred for 40 minutes and further stirred with heating at 40° C. overnight. After the reaction mixture was poured into 100 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 ethanol to give 157 mg of a black crystal having a mp of 125-130° C. (yield: 31.7%).
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-77753e04cf7442b29f50ed8998c89950 |
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| Source note | uspto-grants-2014_09 |
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