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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070427Generated: November 2, 2026

Ethyl cyanoacetate → Ethyl 2-cyano-4-(2,6-difluorophenyl)-4-oxobutanoate

https://huagongshe.com/reaction/2070427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-Difluorophenacyl bromideHCID 2778263—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-cyano-4-(2,6-difluorophenyl)-4-oxobutanoateHCID 6697457381%

Reaction Steps

To a solution of ethyl cyanoacetate (7.24 g) and diisopropylethylamine (19.9 g) in tetrahydrofuran (30 mL) was added dropwise a solution of 2-bromo-1-(2,6-difluorophenyl)ethanone (15.16 g) in tetrahydrofuran (15 mL) at 10-15° C. The mixture was stirred at room temperature for 12 hr. The reaction mixture was filtered, and the obtained filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed successively with water, 1 mol/L hydrochloric acid and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→3:2) to give the title compound as a pale-green oil (yield 13.8 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299261B2
Source datasetuspto-grants-2012_10
ORD IDord-c569d6f779944d6e96f77f95315865f4
Source noteuspto-grants-2012_10