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HRID 241981생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,6-Difluorobenzoic acidHCID 9796—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Potassium ethyl malonateHCID 3446434—
반응물Magnesium ChlorideHCID 5360315—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoateHCID 13550002—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653079B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-aa0c7c90c9db4181bb4de98653e3f5ed
출처 메모uspto-grants-2014_02