Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | 1,2-Bis(dibromomethyl)benzene | HCID 83234 | — |
| Edukt | Fumaronitrile | HCID 637930 | — |
| Edukt | Sodium Bisulfite | HCID 23665763 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2,3-Dicyanonaphthalene | HCID 601270 | 73% |
Reaktionsschritte
One hundred grams (0.67 mole) of sodium iodide was added to a well-stirred solution of 42.2 g (0.1 mole) of α,α,α',α'-tetrabromo-o-xylene and 13.5 g (0.173 mole) of fumaronitrile in 400 ml of anhydrous N,N-dimethylformamide, and the resulting mixture was stirred at 75° C. for about 7 hours in an atmosphere of nitrogen. After the reaction, the mixture was poured into about 2 kg of ice, and thereto was slowly added sodium hydrogen sulfite until the red-brown colored aqueous solution turned to light yellow. After adding a slightly excessive quantity of sodium hydrogen sulfite, the resulting mixture was stirred for a while and then allowed to stand overnight at room temperature. The deposited light yellow-colored solid product was collected by filtration with suction, thoroughly washed with water, and allowed to dry. The light yellow-colored solid product thus obtained was recrystallized from ethanol/chloroform mixture to obtain 13 g (73%) of 2,3-dicyanonaphthalene as a colorless crystalline material.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05188922 |
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| Quelldatensatz | uspto-grants-1993_02 |
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| ORD ID | ord-1e55558865f74cd4952cee46b45e521f |
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| Quellennotiz | uspto-grants-1993_02 |
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