2,4,6-Trifluoroaniline → HCID 178471959, compound
Reaction equation
[F:1][C:2]1[CH:8]=[C:7]([F:9])[CH:6]=[C:5]([F:10])[C:3]=1[NH2:4].[Cl:11][C:12]1[N:29]=[C:28]([Cl:30])[C:27]([F:31])=[CH:26][C:13]=1[C:14]([C:16](=[CH:22]OCC)[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[O:15]>C1(C)C=CC=CC=1>[Cl:11][C:12]1[N:29]=[C:28]([Cl:30])[C:27]([F:31])=[CH:26][C:13]=1[C:14]([C:16](=[CH:22][NH:4][C:3]1[C:2]([F:1])=[CH:8][C:7]([F:9])=[CH:6][C:5]=1[F:10])[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[O:15]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
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.
Workup
- distillationThe solvent was distilled off
- additionto the residue, ethanol was added
- filtrationThe resulting crystals were collected by filtration
- washwashed with diethyl ether
Sources & evidence
- ORD record
- ord-35a21c4dc7d245d38cfbfecafcad9e0f
- Source dataset
- uspto-grants-1999_06
- Patent number
- US05910498
Reaction notes
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