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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163581Generated: November 4, 2026

Diethyl Oxalate → HCID 135705328, compound

https://huagongshe.com/reaction/2163581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantHCID 22752815HCID 22752815—
SolventHexaneHCID 8058—
ProductHCID 135705328HCID 135705328—

Reaction Conditions

Temperature160 °C

Reaction Steps

Diethyl oxalate (47.5 g., 0.326 mole) and 7-fluoro-2-aminoquinoline-3-carboxamide (3.7 g., 0.015 mole) are mixed together and heated at 160° C. for seven hours. The reaction mixture is cooled to room temperature, hexane (300 ml.) added, and the brown solid which precipitates filtered off, and washed with hexane (60 ml.). It is then slurried in hot chloroform (250 ml.) and the insoluble material removed by filtration. The hot filtrate is decolorized with charcoal, filtered and dried (Na2SO4). The light brown solid which precipitates upon cooling is filtered off and recrystallized from isopropyl alcohol. Yield = 1.04 g. (29.2%) of the title ethyl ester. M.P. 248°-251° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134981
Source datasetuspto-grants-1979_01
ORD IDord-48405dd6323440e19e495c4aef5714ed
Source noteuspto-grants-1979_01