Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 69988159 | HCID 69988159 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69987899 | HCID 69987899 | 24.1% |
Reaction Steps
0.78 g (2.00 mmol) of N-ethyl-3-(2-cyano-2-(4-trifluoromethylphenyl)ethenyl) carbazole and 10 ml of N,N-dimethylformamide as solvent were placed in a 200 ml four-necked flask with a mechanical stirrer and bulb-shaped cooler. To this was added an aqueous solution prepared from 0.10 g (2.00 mmol) of sodium cyanide and 1.0 ml of water, which was stirred for 10 minutes. Further, 0.88 g (2.00 mmol) of lead tetraacetate was added. The resultant product was subjected to the reaction for 30 minutes. After the reaction was completed, 100 ml of chloroform was added. To the resultant solution was added 50 ml of water. The resultant liquid was washed in a separatory funnel. To the washed liquid was added sodium sulfate, which was left to stand for 30 minutes and dehydrated. The dehydrated solution was concentrated in an evaporator and dried under vacuum to obtain 0.20 g of a yellow solid. The yield of the synthesized compound was 24%, and its melting point was 180-182° C. The IR chart is shown in FIG. 17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06528657B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-6d07a612920a4b13a9df816766f17d0f |
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| Source note | uspto-grants-2003_03 |
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