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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-3-methoxyanilineHCID 2774533—
ReactantEthyl 3-(3-chloro-2,4,5-trifluorophenyl)-3-oxopropanoateHCID 10934859—
ReactantEthyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylateHCID 54402571—
SolventChloroformHCID 6212—
ProductHCID 23284662HCID 23284662—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136823
Source datasetuspto-grants-2000_10
ORD IDord-7ea1afee1c1a40c4b8cd6bea0964e751
Source noteuspto-grants-2000_10