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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845026Generated: October 30, 2026

P-Anisidine → HCID 23359023, compound

https://huagongshe.com/reaction/845026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantEthyl 3-ethoxy-2-(2,3,4,5-tetrafluorobenzoyl)acrylateHCID 54346083—
SolventEthanolHCID 702—
ProductHCID 23359023HCID 2335902380.5%

Reaction Steps

A mixture of ethyl 2-(2,3,4,5-tetrafluorobenzoyl)-3-ethoxyacrylate (0.4 g), p-anisidine (0.15 g) and ethanol (4 ml) is stirred at room temperature for 30 minutes. After the reaction, the solvent is distilled off under reduced pressure. To the residue is added anhydrous dioxane (10 ml) and thereto is further added portionwise 60% sodium hydride (60 mg). The mixture is stirred at room temperature for 30 minutes. The reaction mixture is poured into saturated aqueous ammonium chloride, and the mixture is extracted with dichloromethane to give ethyl 6,7,8-trifluoro-1-(4-methoxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylate (0.37 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04755513
Source datasetuspto-grants-1988_07
ORD IDord-3f47cba2e3654375bef6823e0c5e7c91
Source noteuspto-grants-1988_07