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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662030Generated: October 30, 2026

3-Buten-2-one, 4-methoxy- → 1-(4-Fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylic acid

https://huagongshe.com/reaction/1662030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Buten-2-one, 4-methoxy-HCID 94297—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 3-(4-fluoroanilino)-3-oxopropanoateHCID 17097465—
SolventEthanolHCID 702—
Product1-(4-Fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylic acidHCID 21081529—

Reaction Steps

To a 4-necked 3 L round bottom flask, is added EtOH (1500 mL), ethyl 3-(4-fluorophenylamino)-3-oxopropanoate (139 g, 617 mmol), sodium ethoxide (65.6 g, 925 mmol) and 4-methoxy-3-buten-2-one (103 g, 925 mmol). The mixture is refluxed for 3 hours. After the solution is cooled to RT, the reaction mixture is concentrated under reduced pressure to remove the EtOH. The residue is diluted with DCM (700 mL) and 1 M HCl (1500 mL). The aqueous phase is extracted with DCM (3×500 mL). The combined organic extracts are washed with saturated aqueous sodium chloride (1000 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue is triturated with EtOAc (150 mL) at RT (10-15° C.) for 1 hour. After filtration and washing with EtOAc (50 mL), 1-(4-fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylic acid is obtained as a yellow solid (85.3 g, 56% yield). MS (m/z): 248 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030302B2
Source datasetuspto-grants-2011_10
ORD IDord-489bd0b1618d4754ae3f655517d9fb5d
Source noteuspto-grants-2011_10