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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820853Generated: October 26, 2026

Hydrochloric Acid → Ethyl 3-(4'-chlorobiphenyl-4-yl)-3-oxopropionate

https://huagongshe.com/reaction/1820853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPropanedioic acid, monoethyl esterHCID 3595298—
Reactant4'-Chlorobiphenyl-4-carbonyl chlorideHCID 9834814—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(4'-chlorobiphenyl-4-yl)-3-oxopropionateHCID 57892092—

Reaction Conditions

Temperature-65 °C

Reaction Steps

4.29 g (32.5 mmol) of monoethyl malonate is dissolved in 100 mL of THF and 42.3 mL (67.7 mmol) of butyllithium solution (1.6N in hexane) is added dropwise at −60° C. The temperature is allowed to come up to −15° C., then the mixture is cooled again to −65° C. and 3.40 g (13.5 mmol) of 4′-chlorobiphenyl-4-carboxylic acid chloride (for preparation see Gazz. Chim. Ital. 1949, 79, 453.) in 30 mL of THF is added dropwise. The mixture is kept for 5 minutes at −65° C., then heated for 2 hours to ambient temperature. The mixture is poured onto 50 mL of 1N hydrochloric acid, extracted with 300 mL of diethyl ether, and the organic phase is washed with saturated sodium hydrogen carbonate solution and water and finally dried over sodium sulfate. The solvent is eliminated, the residue is recrystallized from petroleum ether and the product is dried in vacuo. Yield: 3.10 g (76% of theory); Rf value: 0.60 (silica gel, petroleum ether/ethyl acetate=5:2); m.p. 45° C.-50° C.; C17H15ClO3; EII mass spectrum: m/z=303/305 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605176B2
Source datasetuspto-grants-2009_10
ORD IDord-2c4460cc02c148a684aa9d853e8dc740
Source noteuspto-grants-2009_10