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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226485Generated: October 25, 2026

Hydrochloric Acid → Diethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylmalonate

https://huagongshe.com/reaction/2226485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantMagnesium ethanolateHCID 164963—
Reactant2,4,5-Trifluoro-3-difluoromethoxybenzoyl chlorideHCID 15282971—
SolventDiethyl EtherHCID 3283—
ProductDiethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylmalonateHCID 15023783—

Reaction Steps

Meanwhile, a suspension of diethyl ethoxymagnesium malonate in diethyl ether was prepared from a mixture of 2.80 g (0.0238 moles) of magnesium ethoxide and 3.81 g (0.0238 moles) of diethyl malonate in 60 ml of anhydrous diethyl ether by heating under reflux for 1 hour, whilst stirring. A solution of the 3-difluoromethoxy-2,4,5-trifluorobenzoyl chloride prepared as described above in 50 ml of anhydrous diethyl ether was then added dropwise to the suspension, whilst stirring at room temperature, and the mixture was then stirred at room temperature for an additional 2 hours. 35 ml of 1N aqueous hydrochloric acid were added to the reaction mixture, and the mixture was vigorously stirred. The organic layer was then separated, washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure to give 7.07 g of diethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylmalonate [(XIV), R1 =--OCHF2, R3' =H, R17 =C2H5, X=X'=F] as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348961
Source datasetuspto-grants-1994_09
ORD IDord-9b22b8b2e9884ea4837e15fb9f8d9731
Source noteuspto-grants-1994_09