Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073814Generated: October 26, 2026

Hydrochloric Acid → Ethyl 6-methyl-2,3,4,5-tetrafluorobenzoylacetate

https://huagongshe.com/reaction/2073814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2'-BipyridineHCID 1474—
ReactantMonoethyl malonateHCID 70615—
Reactant2,3,4,5-Tetrafluoro-6-methylbenzoyl chlorideHCID 14651256—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 6-methyl-2,3,4,5-tetrafluorobenzoylacetateHCID 1477410076%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A solution of 10.1 g (76.5 mmol) of malonic acid monoethylester, bipyridyl (catalytic), and 200 ml of dry THF was cooled to -35° C. under argon, treated with 52 ml of 1.5M n-butyllithium (78 mmol), and warmed to -5° C. To this mixture was added 52 ml of 1.5M n-butyllithium (78 mmol) until a pale pink color persisted for 10 minutes. The suspension was cooled to -78° C. and was treated with a solution of 8.8 g (38.8 mmol) of 2,3,4,5-tetrafluoro-6-methylbenzoyl chloride in 100 ml of dry THF. The reaction mixture was stirred at -78° C. for 45 minutes, then warmed to -35° C. and poured into a mixture of ice and 1N hydrochloric acid (77 ml). The organic layer was washed with 5% sodium bicarbonate solution, 3M hydrochloric acid, and water and dried over magnesium sulfate. Concentration gave an orange oil which was chromatographed on silica gel (E. Merck 230-400 Mesh), eluting with 80:20 chloroform:ethyl acetate, to give 8.2 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920120
Source datasetuspto-grants-1990_04
ORD IDord-c873e5700fbf4b78bd0db59754c4b10a
Source noteuspto-grants-1990_04