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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280099Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/280099

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktDiethyl MalonateHCID 7761—
Edukt2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
EduktMagnesiumHCID 5462224—
EduktAcetone cardiceHCID 18522661—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioateHCID 1356497399,7%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04588726
Quelldatensatzuspto-grants-1986_05
ORD IDord-90bbe3f4fd9e405e8245510b2b0900fc
Quellennotizuspto-grants-1986_05