HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369266Generated: October 28, 2026
4-Fluoro-3-methoxyaniline → HCID 23284662, compound
https://huagongshe.com/reaction/369266
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluoro-3-methoxyaniline | HCID 2774533 | — |
| Reactant | Ethyl 3-(3-chloro-2,4,5-trifluorophenyl)-3-oxopropanoate | HCID 10934859 | — |
| Reactant | Ethyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylate | HCID 54402571 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23284662 | HCID 23284662 | — |
Reaction Steps
4-Fluoro-3-methoxyaniline (1.4 g) was added to a chloroform solution (10 ml) with ethyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylate synthesized from ethyl 3-chloro-2,4,5-trifluorobenzoylacetate (2.8 g) in accordance with a method known per se in the art dissolved therein. The reaction mixture was concentrated under reduced pressure, and anhydrous potassium carbonate (2.7 g) and N,N-dimethylformamide (6 ml) were added to the residue, followed by stirring at 90° C. for 15 minutes. The reaction mixture was allowed to cool, and chloroform (80 ml) and distilled water (300 ml) were added to the reaction mixture, thereby conducting liquid separation. A chloroform layer was washed twice with distilled water (300 ml), dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. Deposits were dispersed in ethanol, collected by filtration and washed with ethanol and diisopropyl ether in that order to obtain the title compound (2.98 g) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06136823 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-7ea1afee1c1a40c4b8cd6bea0964e751 |
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| Source note | uspto-grants-2000_10 |
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