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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 637287생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/637287

반응식

참여 물질

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

반응 단계

24.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. Thereafter, the mixture is heated to 50°-60° C. for a further hour, and cooled to -5° C. to -10° C. with dry ice acetone, and a solution of 212.5 g of 2,3,4,5-tetrafluorobenzoyl chloride (1) in 80 ml of absolute toluene is slowly added dropwise at this temperature. The mixture is stirred for 1 hour at 0° to -5° C., and is allowed to reach room temperature overnight, and a mixture of 400 ml of ice water and 25 ml of concentrated sulphuric acid is allowed to run in whilst cooling with ice. The phases are separated, and extraction with toluene is repeated twice. The combined toluene solutions are washed with saturated NaCl solution and dried with Na2SO4, and the solvent is stripped off in vacuo. 335 g of diethyl 2,3,4,5-tetra-fluorobenzoylmalonate (3) are obtained as a crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04556658
출처 데이터셋uspto-grants-1985_12
ORD IDord-c1be0238ed7b471b99e4c73dbf8161fe
출처 메모uspto-grants-1985_12