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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548414Generated: October 30, 2026

3-(Trifluoromethyl)aniline → HCID 9924935, compound

https://huagongshe.com/reaction/548414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-6-nitroquinoline-3-carbonitrileHCID 11085690—
SolventEthanolHCID 702—
ProductHCID 9924935HCID 992493566.6%

Reaction Steps

A mixture of 10.6 g (45.7 mmol) of 4-chloro-6-nitro-quinoline-3-carbonitrile and 8.82 g (54.8 mmol) of 3-(trifluoromethyl)aniline in 270 mL of ethanol was refluxed under N2 for 5 h. The reaction was diluted with ethanol, neutralized with satd sodium bicarbonate and evaporated. The residue was slurried with hexane, collected, washed with hexane and water and dried in vacuo (60° C.) to give 10.9 g of yellow solid. A 2.00 g sample was recrystallized from ethanol to give 1.20 g of bright yellow solid; mp 260-261° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE042376E1
Source datasetuspto-grants-2011_05
ORD IDord-96e660626b2942a692b48988b37b5da4
Source noteuspto-grants-2011_05