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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55073Erstellt: 23. Oktober 2026

4-Aminothiophenol → 4-(4-Aminophenylthio)-7-trifluoromethylquinoline

https://huagongshe.com/de/reaction/55073

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminothiophenolHCID 14510—
Edukt4-Chloro-7-(trifluoromethyl)quinolineHCID 67668—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelEthanolHCID 702—
Produkt4-(4-Aminophenylthio)-7-trifluoromethylquinolineHCID 1897167174,1%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624937
Quelldatensatzuspto-grants-1997_04
ORD IDord-3f3c49436bc044d2a8d9d94e039ec63e
Quellennotizuspto-grants-1997_04