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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241981Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/241981

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2,6-Difluorobenzoic acidHCID 9796—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktPotassium ethyl malonateHCID 3446434—
EduktMagnesium ChlorideHCID 5360315—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 3-(2,6-difluorophenyl)-3-oxopropanoateHCID 13550002—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653079B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-aa0c7c90c9db4181bb4de98653e3f5ed
Quellennotizuspto-grants-2014_02