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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904593Generated: October 31, 2026

Hydrochloric Acid → Ethyl 3-(4-bromo-2,3,5,6-tetrafluorophenyl)-3-oxopropanoate

https://huagongshe.com/reaction/1904593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Bromo-2,3,5,6-tetrafluorobenzoyl chlorideHCID 2783245—
ReactantPropanedioic acid, monoethyl esterHCID 3595298—
ReactantButyllithiumHCID 178418339—
Catalyst2,2'-BipyridineHCID 1474—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(4-bromo-2,3,5,6-tetrafluorophenyl)-3-oxopropanoateHCID 997470586.9%

Reaction Steps

n-Butyllithium (192 ml, 2.4M in hexane) was slowly added to a stirred solution of 30.24 g monoethylmalonate and 15 mg 2,2'-bipyridine in 500 ml tetrahydrofuran cooled to -60° to -70° C. under nitrogen. After about half of the butyllithium had been added, the temperature of the mixture was raised to -20° to -25° C. at which temperature the remainder of the butyllithium was added. The reaction mixture was then recooled to -60° to -70° C. and 33.41 g 4-bromo-2,3,5,6-tetrafluorobenzoyl chloride in 10 ml tetrahydrofuran was added. The reaction mixture was allowed to warm to room temperature, stirred overnight, and then poured into 460 ml 1M hydrochloric acid. The organic layer was separated, dried (magnesium sulfate) and concentrated. The residue was dissolved in ether, washed with aqueous potassium bicarbonate solution, dried (magnesium sulfate), concentrated and distilled to give 34.18 g ethyl 4-bromo-2,3,5,6-tetrafluorobenzoylacetate, b.p. 112°-117° C.(0.8 mm.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839355
Source datasetuspto-grants-1989_06
ORD IDord-d5d67c1bf99f4aa39c3bf2d2d717f6a3
Source noteuspto-grants-1989_06