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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749486Generated: October 26, 2026

Ethyl trimethylsilyl malonate → Ethyl 3-[2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)phenyl]-3-oxopropionate

https://huagongshe.com/reaction/749486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trimethylsilyl malonateHCID 87655—
Reactant2,4-Dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoyl chlorideHCID 86600258—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-[2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)phenyl]-3-oxopropionateHCID 68799347—

Reaction Conditions

Temperature-75 °C

Reaction Steps

1.4 ml of a 1.6 M solution of butyllithium in hexane was added to a solution of 3.47 g (17.0 mmol) of ethyl trimethylsilyl malonate in 45 ml of diethyl ether at −75° C. in such a way that the temperature did not rise above −60° C. The mixture was then stirred at −75° C. for 30 minutes. The 2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoyl chloride was dissolved in 45 ml of dimethoxyethane and added dropwise in 40 minutes. The mixture was slowly warmed to 10° C. and stirred at this temperature for 2.5 hours. The reaction mixture was diluted with ethyl acetate and washed twice each with 250 ml portions of water and saturated sodium bicarbonate solution. The organic phase was dried and concentrated. 3.88 g of the crude mixture were obtained and were reacted without further purification in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402674B2
Source datasetuspto-grants-2008_07
ORD IDord-137ca073d3944f19b6d5b0a457ad8aa8
Source noteuspto-grants-2008_07