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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655219Generated: October 27, 2026

Hydrochloric Acid → 2-(5,7-Difluoro-quinolin-6-yl)-malonic acid diethyl ester

https://huagongshe.com/reaction/655219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant1,4-DioxaneHCID 31275—
ReactantPropanedioic acid, monoethyl esterHCID 3595298—
Reactant6-Bromo-5,7-difluoroquinolineHCID 45108354—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
Product2-(5,7-Difluoro-quinolin-6-yl)-malonic acid diethyl esterHCID 6852956935.4%

Reaction Steps

Ethyl malonate (9.28 g, 8.8 mL, 58.0 mmol) was added dropwise to a mixture of sodium hydride (60 percent in mineral oil, 2.32 g, 58.0 mmol) in 1,4-dioxane (29 mL) at 60° C. CuBr (4.176 g, 29.0 mmol) and 6-bromo-5,7-difluoro-quinoline (7.07 g, 29.0 mmol) were then added and the mixture heated to reflux for 16 h. After such time concentrated hydrochloric acid was added under ice-cooling and then tert-butyl methyl ether and water were added. The separated organic layer was washed with (10%) hydrochloric acid and water sequentially. Dried over sodium sulfate and concentrated. The residue was purified by column chromatography to afford the title compound (3.13 g, 35.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071581B2
Source datasetuspto-grants-2011_12
ORD IDord-139f0a285d1d4b75a767d828dfde68f2
Source noteuspto-grants-2011_12