Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249292Generated: October 25, 2026

Hydrochloric Acid → 2-Chloro-4,5-difluoro-alpha-oxobenzenepropanoic acid ethyl ester

https://huagongshe.com/reaction/249292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantMonoethyl malonateHCID 70615—
Reactant2-Chloro-4,5-difluorobenzoyl chlorideHCID 10198217—
ReactantButyllithiumHCID 178418339—
Product2-Chloro-4,5-difluoro-alpha-oxobenzenepropanoic acid ethyl esterHCID 5366247387%

Reaction Steps

Malonic acid monoethyl ester (26 g, 199 mmol) was dissolved in tetrahydrofuran (500 ml) and cooled to -70°. After the addition of n-butyllithium (112.5 ml of a 1.6M solution in hexanes, 180 mmol), the reaction mixture was allowed to warm to -10°, and additional n-butyllithium was added (112.5 ml, as above). The resulting milky-white mixture was cooled to -70°, and treated with 2-chloro-4,5-difluorobenzoyl chloride (19 g, 90 mmol) in tetrahydrofuran (200 ml). After warming to room temperature, the reaction mixture was allowed to stir for an additional 2 hours, then poured into 2N hydrochloric acid (750 ml). The aqueous mixture was extracted with ethyl ether, and the combined organic layers were dried and concentrated to provided the title product as a light amber oil (20.6 g, 78.6 mmol, 87% yield), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214051
Source datasetuspto-grants-1993_05
ORD IDord-cc154107360447a69a8aee6f0142cf3b
Source noteuspto-grants-1993_05