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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280099생성일: 2026년 10월 25일

Sulfuric Acid → 1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioate

https://huagongshe.com/reaction/280099

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Diethyl MalonateHCID 7761—
반응물2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
반응물MagnesiumHCID 5462224—
반응물Acetone cardiceHCID 18522661—
용매EthanolHCID 702—
용매TolueneHCID 1140—
용매Carbon TetrachlorideHCID 5943—
생성물1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioateHCID 1356497399.7%

반응 단계

24.3 g of magnesium turnings are suspended in 50 ml of anhydrous ethanol. 5 ml of carbon tetrachloride are added and, when the reaction has started, a mixture of 160 g of diethyl malonate, 100 ml of absolute ethanol and 400 ml of anhydrous toluene is added dropwise at 50°-60° C. The mixture is then heated at 50°-60° C. for 1 hour, cooled to 5° C. to -10° C. with dry ice/acetone and, at this temperature, a solution of 212.5 g of 2,3,4,5-tetrafluorobenzoyl chloride in 80 ml of absolute toluene is slowly added dropwise. The mixture is stirred at 0° to -5° C. for 1 hour, allowed to reach room temperature overnight, and, while cooling in ice, a mixture of 400 ml of ice-water and 25 ml of concentrated sulphuric acid is allowed to run in. The phases are separated and two further extractions with toluene are carried out. The combined toluene solutions are washed with saturated NaCl solution, dried with Na2SO4, and the solvent is removed in vacuo. 335 g of diethyl 2,3,4,5-tetrafluorobenzoylmalonate are obtained as a crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04588726
출처 데이터셋uspto-grants-1986_05
ORD IDord-90bbe3f4fd9e405e8245510b2b0900fc
출처 메모uspto-grants-1986_05