돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 580441생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/580441

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 13564973102.6%

반응 조건

온도60 °C

반응 단계

20.1 g of magnesium chips are suspended in 40 ml of anhydrous ethanol. 4 ml of carbon tetrachloride are added and, when the reaction has started, a mixture of 132.2 g of diethyl malonate, 80 ml of absolute ethanol and 320 ml of anhydrous toluene are added dropwise at 50°-60° C. When the reaction has subsided, the mixture is heated at 60° C. for a further 2 hours and cooled to -5° C. to -10° C. with dry ice/acetone, and a solution of 175.5 g of 2,3,4,5-tetrafluorobenzoyl chloride in 100 ml of absolute toluene is slowly added dropwise at this temperature. The mixture is stirred at 0° C. to -5° C. for 1 hour and is allowed to come to room temperature overnight, and a mixture of 350 ml of ice-wter and 50 ml of concentrated sulphuric acid is run in, while cooling with ice. The phases are separated and the aqueous phase is after-extracted twice with toluene. The combined toluene solutions are washed with saturated sodium chloride solution, and dried with sodium sulphate and the solvent is stripped off in vacuo. 284.8 g of diethyl 2,3,4,5-tetrafluoro-benzoyl-malonate are obtained as the crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04753925
출처 데이터셋uspto-grants-1988_06
ORD IDord-cd1a8c0b4cad4de7af2b35fed6368cd6
출처 메모uspto-grants-1988_06