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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637953Generated: October 31, 2026

Sulfuric Acid → Diethyl 2-(2,4-dichloro-5-fluorobenzoyl)malonate

https://huagongshe.com/reaction/637953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDiethyl MalonateHCID 7761—
Reactant2,4-Dichloro-5-fluorobenzoyl chlorideHCID 2736821—
ReactantMagnesiumHCID 5462224—
ReactantAcetone cardiceHCID 18522661—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
ProductDiethyl 2-(2,4-dichloro-5-fluorobenzoyl)malonateHCID 1332681999.6%

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 up, a mixture of 160 g of diethyl malonate, 100 ml of absolute ethanol and 400 ml of anhydrous ether is added dropwise, vigorous reflux being observed. After the reaction has moderated, the mixture is heated to boiling for 2 hours, then cooled down to -5° C. to -10° C. with dry ice/acetone and, at this temperature, a solution of 227.5 g of 2,4-dichloro-5-fluorobenzoyl chloride (1) in 100 ml of absolute ether 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 the aqueous phase is extracted twice more with ether. The combined ether solutions are washed with saturated NaCl solution, dried with Na2SO4 and the solvent is removed in vacuo. 349.5 g of diethyl 2,4-dichloro-5-fluorobenzoylmalonate (3) are obtained as a reaction product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559342
Source datasetuspto-grants-1985_12
ORD IDord-73cb54668556429d990efd919a97905d
Source noteuspto-grants-1985_12