HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415918Generated: October 27, 2026
Benzenamine, 2-chloro-4-fluoro- → HCID 178471927, compound
https://huagongshe.com/reaction/1415918
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenamine, 2-chloro-4-fluoro- | HCID 75013 | — |
| Reactant | Ethyl 3-(2,4,5-trifluorophenyl)-3-oxo-2-(ethoxymethylene)propanoate | HCID 54008204 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178471927 | HCID 178471927 | — |
Reaction Steps
With ice cooling, 5 ml of a chloroform solution containing 1.2 ml of 2-chloro-4-fluoroaniline was added dropwise to 13 ml of a chloroform solution containing 2.46 g of ethyl 2-(2,4,5-trifluorobenzoyl)-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-(2,4,5-trifluorobenzoyl)-3-(2-chloro-4-fluorophenylamino)acrylate. To 15 ml of a N,N-dimethylformamide solution containing 3.00 g of ethyl 2-(2,4,5-trifluorobenzoyl)-3-(2-chloro-4-fluorophenylamino)acrylate was added 1.03 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 2.74 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-52787acfb65f48819a1e3b50186df657 |
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| Source note | uspto-grants-1999_06 |
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