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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231226Generated: November 2, 2026

Ethanol → HCID 2798034, compound

https://huagongshe.com/reaction/2231226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
Reactant2,4-DifluoroanilineHCID 9709—
SolventHexaneHCID 8058—
ProductHCID 2798034HCID 279803479.5%

Reaction Steps

Into an appropriate reactor fitted with warming, cooling and stirring means, were poured 152.5 ml (1.5 mol) of 2,4-difluoroaniline and 425 ml (2.1 mol) of diethyl ethoxymethylenemalonate. The mixture was warmed at 90° to 100° C. for about three hours with evacuation of ethanol appearing in the condensation. This led to a solid product which was treated with hexane, washed, crystallized from hexane and dried to give 356.5 g (yield 79.5%) of 1-(2,2-diethoxycarbonyl-vinylamino)-2,4-difluoro-benzene. Elemental analysis of the product showed a good correspondence with the formula C14H15NO4F2. 350 g (1.17 mol) of this product were poured into a reactor with 1 liter of diphenyloxide. The mixture was refluxed at 265°-270° C. for 11/2 hours with a subsequent evacuation of the ethanol produced during the cyclisation. After cooling to ambient temperature, there was obtained a residue which was treated with benzene and then with hexane, dried and recrystallized from methanol. This gave 239 g (yiel 80.7%) of 1,4-dihydro-3-ethoxycarbonyl-6,8-difluoro-4-oxo-quinoline, elemental analysis of which showed a good correspondence with the formula C12H9NO3F2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782068
Source datasetuspto-grants-1988_11
ORD IDord-246d898afec9497e8f8a53e09eb0b462
Source noteuspto-grants-1988_11