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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415916Generated: October 25, 2026

2,4,6-Trifluoroaniline → HCID 178471959, compound

https://huagongshe.com/reaction/1415916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrifluoroanilineHCID 67765—
ReactantEthyl 2-(2,6-dichloro-5-fluoronicotinoyl)-3-ethoxyacrylateHCID 54342804—
SolventTolueneHCID 1140—
ProductHCID 178471959HCID 178471959—

Reaction Steps

With ice cooling, 5 ml of a toluene solution containing 1.39 ml of 2,4,6-trifluoroaniline was added dropwise to 10 ml of a toluene solution containing 6.40 g of ethyl 2-(2,6-dichloro-5-fluoronicotinoyl)-3-ethoxyacrylate and stirred overnight at room temperature. The solvent was distilled off then to the residue, ethanol was added. The resulting crystals were collected by filtration and washed with diethyl ether, to give ethyl 2,6-dichloro-5-fluoronicotinoyl-3-(2,4,6-trifluorophenyl)aminoacrylate. To 9 ml of a N,N-dimethylformamide solution containing 2.0 g of ethyl 2,6-dichloro-5-fluoronicotinoyl-3-(2,4,6-trifluorophenylamino)acrylate was added 0.63 g of potassium carbonate. The solution was stirred for 90 minutes at room temperature. The reaction solution was poured into ice water, the precipitated solid was collected by filtration and washed with ethanol and diethyl ether, to give 1.38 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910498
Source datasetuspto-grants-1999_06
ORD IDord-35a21c4dc7d245d38cfbfecafcad9e0f
Source noteuspto-grants-1999_06