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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722252Generated: November 1, 2026

Methyl iodide → Ethyl 1-methyl-4-oxo-7-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/1722252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178469560HCID 178469560—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-methyl-4-oxo-7-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylateHCID 20028483—

Reaction Steps

A mixture of ethyl 4-hydroxy-7-trifluoromethylquinoline-3-carboxylate (370.5 g), anhydrous potassium carbonate (179.4 g), iodomethane (202.4 g) and anhydrous dimethylformamide (2 liters) was stirred at room temperature overnight. More dimethylformamide (500 ml) was added and stirring was continued for 24 hours. The dimethylformamide was distilled off in vacuo and water (2 litres) was added to the residue. The resulting solid was collected, washed with water, dried and recrystallised from IMS to give the novel compound ethyl 1-methyl-4-oxo-7-trifluoromethyl-1,4-dihydroquinoline-3-carboxylate, m.p. 222°-224°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855291
Source datasetuspto-grants-1989_08
ORD IDord-38bea017969548c788f63ef306968e04
Source noteuspto-grants-1989_08