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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369247Generated: October 28, 2026

4-Fluoro-3-methoxyaniline → HCID 23284696, compound

https://huagongshe.com/reaction/369247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-3-methoxyanilineHCID 2774533—
ReactantEthyl 3-oxo-3-(2,4,5-trifluoro-3-methylphenyl)propanoateHCID 14052572—
ReactantHCID 53656353HCID 53656353—
SolventChloroformHCID 6212—
ProductHCID 23284696HCID 23284696—

Reaction Conditions

Temperature90 °C

Reaction Steps

4-Fluoro-3-methoxyaniline (1.4 g) was added to a chloroform solution (10 ml) of ethyl 3-ethoxy-2-(2,4,5-trifluoro-3-methylbenzoyl)acrylate synthesized from ethyl 2,4,5-trifluoro-3-methylbenzoylacetate (2.6 g) in accordance with a method known per se in the art. The mixture was concentrated under reduced pressure, and anhydrous potassium carbonate (3.0 g) and N,N-dimethylformamide (7 ml) were added to the residue, followed by stirring at 90° C. for 15 minutes. The reaction mixture was allowed to cool, and chloroform (100 ml) and distilled water (250 ml) were added to the mixture, thereby conducting liquid separation. A chloroform layer was then washed twice with distilled water (250 ml), dried over anhydrous magnesium sulfate and 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 (2.59 g) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136823
Source datasetuspto-grants-2000_10
ORD IDord-a7ec8c2365cb461484695ae3ac638dbf
Source noteuspto-grants-2000_10