Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | 3-Nitrocarbazole | HCID 76503 | — |
| Catalyst | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 14251393 | HCID 14251393 | — |
Reaction Steps
21.2 g (0.1 mol) 3-nitrocarbazole were suspended in 250 ml benzene in a three-necked flask equipped with stirrer, condenser and thermometer and present in an oil-bath, then mixed with 50 ml acrylonitrile, heated to 50°C and, after the addition of two drops of benzyl trimethyl ammonium hydroxide, reacted for two hours at 70°C, while stirring. After evaporation of the reaction mixture and recrystallization of the residue from aqueous acetone, there were obtained 22 g 9-(β-cyanoethyl)-3-nitrocarbazole, which was further worked up directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03947377 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-30bb131a184e42c2a00676ab1349d316 |
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| Source note | uspto-grants-1976_03 |
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