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HRID 241981作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2,6-Difluorobenzoic acidHCID 9796—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物Potassium ethyl malonateHCID 3446434—
反応物Magnesium ChlorideHCID 5360315—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoateHCID 13550002—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653079B2
出典データセットuspto-grants-2014_02
ORD IDord-aa0c7c90c9db4181bb4de98653e3f5ed
出典メモuspto-grants-2014_02