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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580441Generated: October 26, 2026

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

https://huagongshe.com/reaction/580441

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 13564973102.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753925
Source datasetuspto-grants-1988_06
ORD IDord-cd1a8c0b4cad4de7af2b35fed6368cd6
Source noteuspto-grants-1988_06