HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2050513Erstellt: 25. Oktober 2026
Iodoethane → 4-Ethyl-8-(3-(trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3,5(4H)-dione
https://huagongshe.com/reaction/2050513
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Iodoethane | HCID 6340 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 8-(3-(Trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3,5(4H)-dione | HCID 15044076 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Ethyl-8-(3-(trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3,5(4H)-dione | HCID 20058375 | — |
Reaktionsschritte
To a stirred mixture of 5.0 g of 8-(3-(trifluoromethyl)phenyl)-3H,6H-1,4,5a,8a-tetraazaacenaphthylene-3,5(4H)-dione (prepared as described in Example 14) in 50 ml of dry N,N-dimethylformamide, under nitrogen, is added 800 mg of 60 percent sodium hydride (dispersion in mineral oil). The mixture is stirred at room temperature for 2 hours, then 10 ml of iodoethane is added and stirring is continued for 48 hours. The reaction mixture is evaporated to dryness, then treated with water, and the gummy solid which is isolated is dissolved in chloroform and the extract dried over anhydrous sodium sulfate. Evaporation gives an oil which is triturated with diethyl ether-hexane to provide a yellow solid which is collected by filtration to give 2.0 g of the desired product as a white solid. The product is recrystallized from isopropyl alcohol, mp 161-163° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05013737 |
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| Quelldatensatz | uspto-grants-1991_05 |
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| ORD ID | ord-29f8a411b7dd4c85a46fb10dcf333c92 |
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| Quellennotiz | uspto-grants-1991_05 |
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