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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274443Generated: October 31, 2026

Carbon Tetrachloride → Diethyl 3,4-dimethoxy-5-nitrobenzoylmalonate

https://huagongshe.com/reaction/274443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantDiethyl MalonateHCID 7761—
ReactantMagnesiumHCID 5462224—
Reactant3,4-Dimethoxy-5-nitrobenzoyl chlorideHCID 21928615—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 3,4-dimethoxy-5-nitrobenzoylmalonateHCID 19000155—

Reaction Steps

4.9 g of magnesium are suspended in 15 ml of absolute ethanol and, after adding 1 ml of carbon tetra- chloride, warmed until the reaction starts. A solution of 31.8 g of diethyl malonate in 19.9 ml of absolute ethanol and 80 ml of absolute toluene is then added dropwise while stirring so that the temperature lies between 50° and 60°. The reaction mixture is subsequently stirred at this temperature for an additional 1 hour, whereupon it is cooled to -5° and a solution of 49.3 g of 3,4-dimethoxy-5-nitrobenzoyl chloride (m.p. 82°-85°) in 300 ml of absolute toluene and 50 ml of absolute tetrahydrofuran is added dropwise so that the temperature does not exceed -5°. The mixture is subsequently stirred at room temperature overnight. After distillation of the solvent the residue is dissolved in 500 ml of ethyl acetate. The solution is treated while stirring and cooling with ice with an ice-cold solution of 12 ml of concentrated sulfuric acid in 80 ml of water. The organic phase is washed with sodium chloride solution, dried over magnesium sulfate and evaporated. The oil obtained is chromatographed on a ten-fold amount of silica gel with methylene chloride. The crystalline material obtained is recrystallized from isopropyl ether. There is obtained diethyl 3,4-dimethoxy-5-nitrobenzoylmalonate in the form of pale beige crystals of m.p. 70°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389653
Source datasetuspto-grants-1995_02
ORD IDord-1922e9b955fa4b8f83e14f29f03f4367
Source noteuspto-grants-1995_02