HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Aminothiophenol → 4-(4-Aminophenylthio)-7-trifluoromethylquinoline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Aminothiophenol | HCID 14510 | — |
| Edukt | 4-Chloro-7-(trifluoromethyl)quinoline | HCID 67668 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-(4-Aminophenylthio)-7-trifluoromethylquinoline | HCID 18971671 | 74,1% |
Reaktionsschritte
4-Chloro-7-trifluoromethylquinoline (0.043 moles, 10.0 g), 4-aminothiophenol (0.043 moles, 5.3 g) and 4-dimethylaminopyridine (0.04 moles, 4.9 g) were stirred in 250 ml ethanol for 3 days. The reaction mixture was filtered, concentrated, ethyl acetate added, washed with water and dried over sodium sulfate. The solution was concentrated and the product purified by HPLC over silica gel eluted with 25% ethyl acetate/hexane to yield 4-(4-aminophenylthio)-7-trifluoromethylquinoline 10.2 g, 74%. Mass Spec (FD) 320. Calculated for C16H11F3N2S: C, 59.99; H, 3.46; N, 8.74. Found: C, 60.08; H, 3.49; N, 8.77.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05624937 |
| Quelldatensatz | uspto-grants-1997_04 |
| ORD ID | ord-3f3c49436bc044d2a8d9d94e039ec63e |
| Quellennotiz | uspto-grants-1997_04 |