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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266548Generated: October 27, 2026

Hydrochloric Acid → HCID 54118611, compound

https://huagongshe.com/reaction/266548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantMagnesiumHCID 5462224—
Reactant2-Nitro-4-(trifluoromethyl)benzoyl chlorideHCID 14323524—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 54118611HCID 5411861196.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of magnesium turnings (4.94 g) and carbon tetrachloride (2 ml) in ethanol (35 ml) was warmed to 50° C. until the reaction started. Diethyl ether (150 ml) was then added cautiously, with stirring. A solution of diethyl malonate (32.5 g) in diethyl ether (50 ml) was then added dropwise, then stirred and heated at reflux for 2 hours. After cooling the mixture, diethyl ether (150 ml) was added. A solution of 2-nitro-4-trifluoromethylbenzoyl chloride (50.7 g) in diethyl ether (100 ml) was added dropwise. The mixture was heated at reflux for 2 hours. After cooling, hydrochloric acid (2M,200 ml) was added and the layers were separated. The organic layer was washed with water, dried (anhydrous sodium sulphate), and filtered. The filtrate was evaporated to dryness, to give diethyl 2-nitro-4-trifluoromethylbenzoylmalonate (72.6 g), in the form of an off-white solid, m.p. 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650533
Source datasetuspto-grants-1997_07
ORD IDord-b653957c0a7443a0b7b9692037e38a2d
Source noteuspto-grants-1997_07