Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788665Generated: November 2, 2026

P-Anisidine → HCID 23359023, compound

https://huagongshe.com/reaction/1788665

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 resulting residue is added anhydrous dioxane (10 ml) and further added portionwise 60% sodium hydride (60 mg). The mixture is stirred at room temperature for 30 minutes. Thereafter, the reaction mixture is poured into saturated aqueous ammonium chloride and then 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 numberUS04684648
Source datasetuspto-grants-1987_08
ORD IDord-a9304fd128cd465193acaec345266e54
Source noteuspto-grants-1987_08