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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241981Generated: October 25, 2026

Hydrochloric Acid → Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate

https://huagongshe.com/reaction/241981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,6-Difluorobenzoic acidHCID 9796—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantPotassium ethyl malonateHCID 3446434—
ReactantMagnesium ChlorideHCID 5360315—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(2,6-difluorophenyl)-3-oxopropanoateHCID 13550002—

Reaction Steps

A mixture of 2,6-difluorobenzoic acid (15 g, 0.095 mol) and carbonyldiimidazole (18 g, 0.14 mol, 1.5 equiv) in anhydrous tetrahydrofuran (150 mL) was stirred at ambient temperature for 6 hours. In a separate flask, a suspension of anhydrous magnesium(II) chloride (9.0 g, 0.095 mol, 1.0 equiv) and potassium ethyl malonate (22 g, 0.13 mol, 1.4 equiv) in tetrahydrofuran (225 mL) was stirred at 50-60° C. for 6 hours, cooled to ambient temperature, which was then added via syringe to the solution of activated acid, and the mixture was stirred for an additional 18 hours at ambient temperature. The mixture was refluxed for 3 hours, cooled to ambient temperature, poured into water and acidified with hydrochloric acid (12 N aqueous) to pH<2. The aqueous layer was extracted with ethyl acetate and the organic extract was washed with water, dried with sodium sulfate, filtered and concentrated in vacuo, providing the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653079B2
Source datasetuspto-grants-2014_02
ORD IDord-aa0c7c90c9db4181bb4de98653e3f5ed
Source noteuspto-grants-2014_02