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HRID 36708생성일: 2026년 10월 24일

Sulfuric Acid → Diethyl (2,4-dichloro-3,6-difluorobenzoyl)-malonate

https://huagongshe.com/ko/reaction/36708

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Propanedioic acid, monoethyl esterHCID 3595298—
반응물MagnesiumHCID 5462224—
반응물2,4-Dichloro-3,6-difluorobenzoyl chlorideHCID 15070033—
반응물Acetone cardiceHCID 18522661—
용매EthanolHCID 702—
용매TolueneHCID 1140—
용매Carbon TetrachlorideHCID 5943—
생성물Diethyl (2,4-dichloro-3,6-difluorobenzoyl)-malonateHCID 15070034—

반응 조건

온도70 °C

반응 단계

2.1 g of magnesium filings are suspended in 5 ml of anhydrous ethanol. 0.5 ml of carbon tetrachloride is added and, when the reaction has started, a mixture of 14 g of ethyl malonate, 10 ml of absolute ethanol and 41 ml of toluene is added dropwise. The mixture is then heated at 70° C. for a further 1.5 hours and cooled to -5° C. to -10° C. with acetone/dry ice, and a solution of 21.5 g of 2,4-dichloro-3,6-difluorobenzoyl chloride in 30 ml of toluene is slowly added dropwise at this temperature. The mixture is stirred at 0° C. for 1 hour and allowed to come to room-temperature overnight, and a mixture of 35 ml of ice-water and 5 ml of concentrated sulphuric acid is allowed to run in, while cooling with ice. The phases are separated and subsequent extraction is carried out twice with toluene. The combined toluene solutions are washed once with saturated sodium chloride solution and dried with Na2SO4 and the solvent is stripped off in vacuo. 34.7 g of diethyl (2,4-dichloro-3,6-difluorobenzoyl)-malonate are obtained as a crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05416096
출처 데이터셋uspto-grants-1995_05
ORD IDord-5bb3b32bdb704fd983c8dbcf3efbdc17
출처 메모uspto-grants-1995_05