Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methane | HCID 297 | — |
| Edukt | Chloroacetonitrile | HCID 7856 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Cyanophenol | HCID 13019 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | 1,1,1-Trichloroethane | HCID 6278 | — |
| Produkt | 4-(Cyanomethoxy)benzonitrile | HCID 20529061 | — |
Reaktionsschritte
The compound of 4-cyanophenoxyacetonitrile was prepared by heating 29.8 g of 4-cyanophenol, 44.8 g of anhydrous K2CO3, 40 ml of dimethylformamide and 18.75 g of chloroacetonitrile with stirring in a round-bottomed three-necked flask at 70°-80° C. for 3 hours, after which time the reaction mixture was poured into an ice and water mixture, which resulted in crystal formation. The crystals were separated by filtering and were then washed with water. After drying a pale tan solid was obtained which was then dissolved in methylchloroform at reflux temperature, treated with activated charcoal and filtered. The filtrate was cooled to 5° C. and the resulting crystals filtered and dried to give the 4-cyanophenoxyacetonitrile.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04343808 |
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| Quelldatensatz | uspto-grants-1982_08 |
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| ORD ID | ord-00053850eedf48998b805479552470f3 |
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| Quellennotiz | uspto-grants-1982_08 |
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