Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | O-Xylene | HCID 7237 | — |
| Edukt | Methyl Acrylate | HCID 7294 | — |
| Edukt | Benzeneacetonitrile, 4-fluoro- | HCID 68016 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Produkt | 1-(4-Fluorophenyl)-4-oxocyclohexanecarbonitrile | HCID 91805 | — |
Reaktionsschritte
A mixture of 221 parts of 4-fluorobenzeneacetonitrile, 700 parts of sodium methoxide solution 30% and 900 parts of dimethylbenzene was stirred for 5 minutes. Then there were added dropwise 309 parts of methyl 2-propenoate (exothermic reaction: temperature rose to 65° C.). Upon completion, stirring was continued overnight at reflux temperature. The methanol was distilled off till an internal temperature of 110° C. was reached. After cooling, 1000 parts of a hydrochloric acid solution 6N were added dropwise and the whole was stirred and refluxed for 5 minutes. Upon cooling, the layers were separated. The organic phase was dried, filtered and evaporated. The residue was stirred and refluxed for 4 hours together with 500 parts of acetic acid, 500 parts of water and 500 parts of a hydrochloric acid solution. After cooling, the product was extracted with trichloromethane. The extract was washed successively with water, with a diluted sodium hydroxide solution and again with water till neutralization, dried, filtered and evaporated. The residue was crystallized from 2-propanol, yielding 134.5 parts of 1-(4-fluorophenyl)-4-oxocyclohexanecarbonitrile; mp. 91.8° C. (intermediate 1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05001125 |
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| Quelldatensatz | uspto-grants-1991_03 |
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| ORD ID | ord-f87bb568ddf449ee9d83b9b9813a5e7b |
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| Quellennotiz | uspto-grants-1991_03 |
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