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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280099Generated: October 25, 2026

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

https://huagongshe.com/reaction/280099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDiethyl MalonateHCID 7761—
Reactant2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
ReactantMagnesiumHCID 5462224—
ReactantAcetone cardiceHCID 18522661—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventCarbon TetrachlorideHCID 5943—
Product1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioateHCID 1356497399.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588726
Source datasetuspto-grants-1986_05
ORD IDord-90bbe3f4fd9e405e8245510b2b0900fc
Source noteuspto-grants-1986_05