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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070693Generated: October 31, 2026

Hydrochloric Acid → Ethyl Alpha-oxo-3-(2-nitro-4,5-dichlorophenyl)propanoate

https://huagongshe.com/reaction/1070693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
Reactant1,2-Dichloro-4-methyl-5-nitrobenzeneHCID 343795—
ReactantPotassiumHCID 5462222—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductEthyl Alpha-oxo-3-(2-nitro-4,5-dichlorophenyl)propanoateHCID 1073340961,984.102%

Reaction Steps

To a suspension of potassium (49.2 g, 1.26 mol) in anhydrous diethyl ether (500 ml), a solution of absolute EtOH (319 ml) and anhydrous diethyl ether (260 ml) was added dropwise under nitrogen during a period of four hours. The resulting solution was diluted with anhydrous diethyl ether (1200 mL) and then diethyl oxalate (171 ml, 1.26 mol) was added dropwise in about 30 minutes. To the resulting yellow mixture, a solution of 2-nitro-4,5-dichlorotoluene (260 g, 1.26 mmol), prepared as described by Cohen and Dakin in J. Chem. Soc., 79, 1133, in anhydrous diethyl ether (450 ml) was added dropwise in one hour at RT. Stirring was continued for additional three hours and the dark-brown mixture was settled at RT for two days. The potassium salt was collected by suction and dried to give a dark-brown powder. This was suspended in a mixture of water (400 ml) and ethyl acetate (400 ml), then acidified with 10% HCl. The organic phase was washed with brine, aqueous sat. NaHCO3 and again brine, then it was dried with MgSO4. Evaporation produced 239 g of title compound (781 mmol, yield 62.0%) as a light brown solid that was used as such for the next step, m.p.=92-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903117B2
Source datasetuspto-grants-2005_06
ORD IDord-7942beb3fef64f6780ed0a0abb81858c
Source noteuspto-grants-2005_06