Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Chlorobenzoic Acid | HCID 447 | — |
| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | 2-Oxocyclohexanepropiononitrile | HCID 96223 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 3-Chlorobenzoic Acid | HCID 447 | — |
| Produkt | 3-(7-Oxooxepan-2-yl)propanenitrile | HCID 11768938 | — |
Reaktionsschritte
A reactor is loaded with 151 g of 3-(2-cyclohexanonyl)propionitrile in 500 ml of n-hexane and 260 g of m-chloroperbenzoic acid (70% titer) dissolved at 50° C. in 2000 ml of n-hexane in 30 minutes. The solution is heated to 55° C. for 15 hours. Cooling separates from the solution, in crystalline form, part of the m-chlorobenzoic acid, which is scarcely soluble in the system, together with a heavy liquid phase which is formed by 7-cyanoethyl-2-oxepanone and by m-chlorobenzoic acid. 71.5 g of 7-cyanoethyl-2-oxepanone, impure with m-chlorobenzoic acid, are recovered from the lower phase. 24 g of 7-cyanoethyl-2-oxepanone are recovered from the upper phase by concentration and by several crystallizations. Conversion with respect to the initial ketone is 85%. Yield on the converted substance is 57%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05670661 |
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| Quelldatensatz | uspto-grants-1997_09 |
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| ORD ID | ord-62b2e574547047a89abd0f996fcfb47e |
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| Quellennotiz | uspto-grants-1997_09 |
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