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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trifluoroaniline | HCID 67765 | — |
| Reactant | Ethyl 2-(2,6-dichloro-5-fluoronicotinoyl)-3-ethoxyacrylate | HCID 54342804 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178471959 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05910498 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-35a21c4dc7d245d38cfbfecafcad9e0f |
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| Source note | uspto-grants-1999_06 |
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