Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | HCID 14348987 | HCID 14348987 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 14349028 | HCID 14349028 | — |
Reaction Steps
A solution of 2,3,4,5-tetrahydro-1-(p-trifluoromethylphenoxy)-3-benzazepine of Example 1 (15 g, 0.049 mole) and acrylonitrile (5.2 g, 0.098 mole) in isopropanol (50 ml) was stirred at reflux (95° C.) for twenty hours. The reaction mixture was cooled then concentrated to an oil (17 g, 96%) of which 3.5 g was distilled to an oil of 3-(2-cyanoethyl)-2,3,4,5-tetrahydro-1-(p-trifluoromethylphenoxy)-3-benzazepine (2.6 g, 235°-237° C./0.1 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04935418 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-0491b1155351466c870b1b6938eb2fd8 |
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| Source note | uspto-grants-1990_06 |
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