Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Aminothiophenol | HCID 14510 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 2,6-Dichloroquinoxaline | HCID 87748 | — |
| Edukt | Potassium p-aminothiophenolate | HCID 11816037 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-(6-Chloro-2-quinoxalylthio)-aniline | HCID 13108942 | 52% |
Reaktionsschritte
5.7 g (0.045 mol) of p-aminothiophenol together with 3 g (0.045 mol) of 86% potassium hydroxide and 2 ml of water in 80 ml of dimethylsulfoxide was heated under stirring at 80°-90° C. for 5 hours to make the potassium p-aminothiophenolate. The water generated was removed off by azeotropic distillation under reduced pressure. To this solution which was allowed to be cooled to room temperature was added a solution of 9 g (0.045 mol) of 2,6-dichloroquinoxaline dissolved in 100 ml of dimethylsulfoxide. The mixture was subjected to the reaction, while stirring, at 80°-90° C. for 8 hours. After the reaction mixture was cooled to the room temperature, it was poured into a great deal of water and stirred. The precipitating solid was filtered off, washed with 5% aqueous solution of sodium hydroxide and then washed with water, followed by drying. The crude crystals thus obtained were recrystallized from a mixed solution of ethanol-benzene to produce 6.7 g (yield 52%) of the intended compound (Compound No. 10) as light-yellow crystals, m.p. 144°-147° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04376202 |
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| Quelldatensatz | uspto-grants-1983_03 |
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| ORD ID | ord-bbabf4cdcf4d43369b8907aa8c120dd8 |
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| Quellennotiz | uspto-grants-1983_03 |
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