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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525888Generated: November 2, 2026

1,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene) → Ethyl 8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/525888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene)HCID 24670—
ReactantDiethyl 2-(((2-fluoro-3,4-dimethoxyphenyl)amino)methylene)malonateHCID 86732752—
SolventHexaneHCID 8058—
ProductDiethyl 2-(((2-fluoro-3,4-dimethoxyphenyl)amino)methylene)malonateHCID 86732752—
ProductEthyl 8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 8673275361%

Reaction Steps

To Dowtherm (25 mL) heated at 250° C. was added diethyl 2-(((2-fluoro-3,4-dimethoxyphenyl)amino)methylene)malonate (10 g, 29.3 mmol). The mixture was stirred at the same temperature for 40 mins. LCMS indicated completion of the reaction. The reaction was allowed to cool at rt for 5 mins and was then poured into cold hexane, the yellow precipitate was collected by filtration, washed with hexane and dried in the air. This reaction was carried out in similar scale for several times. From a total of 72 g of diethyl 2-(((2-fluoro-3,4-dimethoxyphenyl)amino)methylene)malonate (211 mmol), ethyl 8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate (38 g, 129 mmol, 61.0% yield) was obtained as a yellow solid. LCMS (M+H)+: 296.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340556B2
Source datasetuspto-grants-2016_05
ORD IDord-9c8c52ae11254b36a17e745f6d08e698
Source noteuspto-grants-2016_05