Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Nitroaniline | HCID 7475 | — |
Reaction Steps
A mixture of 120 parts of acrylonitrile and 1000 parts of acetone is introduced into the solution of the diazo derivative obtained from 276 parts of p-nitraniline. Then 40 parts of cupric chloride cyrstallised with 2 molecules of water are added and the mixture is kept vigorously stirred. The evolution of nitrogen is exothermal and the temperature must be maintained at 30°-32° C. by means of a cooling bath. After the diazonium chloride has disappeared (six hours), the yellow flakes which melt at 108° C. are filtered off. After recrystallising from methanol, 330 parts of 2-chloro-4'-nitro-3-phenyl-propionitrile are obtained which melts at 112° C. The product obtained is then dehydrohalogenated by means of 200 parts of crystalline sodium acetate in a mixture of 340 parts of water and 800 parts of ethyl alcohol. The mixture is heated under reflux for 12 hours and 225 parts of 4-nitro-cinnamonitrile which melts at 202° C. are isolated in the cold.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04101543 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-48eaaf55aa40428fa8895faff8c20cde |
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| Source note | uspto-grants-1978_07 |
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