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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703080Generated: October 25, 2026

Sulfuric Acid → Diethyl (2,4-dichloro-5-fluoro-3-nitrobenzoyl)propanedioate

https://huagongshe.com/reaction/703080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDiethyl MalonateHCID 7761—
ReactantMagnesiumHCID 5462224—
ReactantBenzoyl chloride, 2,4-dichloro-5-fluoro-3-nitro-HCID 11818130—
ReactantHCID 178418361HCID 178418361—
CatalystCarbon TetrachlorideHCID 5943—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductDiethyl (2,4-dichloro-5-fluoro-3-nitrobenzoyl)propanedioateHCID 1373313991%

Reaction Steps

2.1 g of carbon tetrachloride are added to 10.1 g of magnesium filings in 21 ml of ethanol and, when the evolution of hydrogen has started, a mixture of 66.6 g of diethyl malonate, 40 ml of ethanol and 150 ml of toluene is added dropwise at 50°-60° C. The mixture is subsequently stirred at this temperature for 1 hour and cooled to -5° to -10° C. and a solution of 109.2 g of 2,4-dichloro-5-fluoro-3-nitro-benzoyl chloride in 50 ml of toluene is slowly added dropwise. The mixture is then stirred at 0° C. for 1 hour, brought to room temperature overnight and warmed at 40°-50° C. for a further 2 hours. A mixture of 160 ml of water and 10.4 ml of concentrated sulphuric acid is added to the reaction mixture, while cooling with ice, and the organic phase is separated off. The aqueous phase is extracted with toluene, the combined organic extract is washed with saturated sodium chloride solution and dried with sodium sulphate and the solvent is stripped off. 144.5 g of diethyl (2,4-dichloro-5-fluoro-3-nitro-benzoyl)-malonate are obtained as a crude product. After adding 200 ml of water and 0.6 g of 4-toluenesulphonic acid, this is heated under reflux for 3 hours, the mixture is extracted with methylene chloride, the extract is dried with sodium sulphate and the solvent is distilled off in vacuo. 118 g of substituted benzoylacetate are obtained as a crude product. It has a sufficient purity for further reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04981854
Source datasetuspto-grants-1991_01
ORD IDord-e42b3c691e2b4bfbbfd675aad13b40bd
Source noteuspto-grants-1991_01