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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55073Generated: October 25, 2026

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

https://huagongshe.com/reaction/55073

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 C16H11F3N2S: 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 numberUS05624937
Source datasetuspto-grants-1997_04
ORD IDord-3f3c49436bc044d2a8d9d94e039ec63e
Source noteuspto-grants-1997_04