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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395329Generated: October 26, 2026

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

https://huagongshe.com/reaction/2395329

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminothiophenolHCID 14510—
Reactant4-Chloro-7-(trifluoromethyl)quinolineHCID 67668—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthanolHCID 702—
Product4-(4-Aminophenylthio)-7-trifluoromethylquinolineHCID 1897167174.1%

Reaction Steps

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 C16H11F3 N2S: C, 59.99; H, 3.46; N. 8.74. Found: C, 60.08; H, 3.49; N, 8.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814646
Source datasetuspto-grants-1998_09
ORD IDord-7e87b8c52cfa43f0819b76fd78d57cb6
Source noteuspto-grants-1998_09