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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963398Generated: October 27, 2026

Sulfuric Acid → Diethyl 2-(2-chloro-4-iodo-benzoyl)-malonate

https://huagongshe.com/reaction/963398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDiethyl MalonateHCID 7761—
ReactantMagnesiumHCID 5462224—
Reactant2-Chloro-4-iodobenzoyl chlorideHCID 19081536—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventCarbon TetrachlorideHCID 5943—
ProductDiethyl 2-(2-chloro-4-iodo-benzoyl)-malonateHCID 1908173596%

Reaction Steps

mb) 4.2 g of magnesium shavings are suspended in 8.3 ml of anhydrous ethanol and treated with 0.83 ml of carbon tetrachloride. A solution of 27.63 g of diethyl malonate in 17 ml of ethanol and 62 ml of toluene is added dropwise in such a manner that the temperature remains at 50°-60°. Subsequently, the mixture is heated at 60° for a further 1 hr. The reaction mixture is cooled to -30° and a solution of 51.9 g 2-chloro-4-iodo-benzoyl chloride in 70 ml of anhydrous toluene is added dropwise within 30 min. The reaction mixture is stirred while slowly warming to room temperature within 1.30 hrs., then cooled to 0° and treated dropwise with a solution of 4 ml of conc. sulphuric acid in 60 ml of water. After 20 min. the phases are separated and the aqueous solution is back-extracted twice with 100 ml of toluene each time. The combined organic phases are washed with 100 ml of saturated, aqueous sodium chloride solution, dried over magnesium sulphate and concentrated. 70.3 g (96%) of diethyl 2-(2-chloro-4-iodo-benzoyl)-malonate are obtained as a yellowish oil. Mass spectrum: peaks inter alia at 424 (M+, 0.4%), 389 (48%), 343 (63%), 265 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763450
Source datasetuspto-grants-1998_06
ORD IDord-a965a8220a764886a45be9542616010b
Source noteuspto-grants-1998_06