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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610454Generated: November 3, 2026

Hydrochloric Acid → Ethyl 3-oxo-3-(4-phenoxyphenyl)propanoate

https://huagongshe.com/reaction/1610454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Phenoxybenzoic acidHCID 19539—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 178472271HCID 178472271—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-oxo-3-(4-phenoxyphenyl)propanoateHCID 2760258180.9%

Reaction Steps

To a solution of 3-phenoxybenzoic acid (13.5 g, 63.0 mmol) in tetrahydrofuran (150 ml) was added 1,1′-carbonylbis-1H-imidazole (11.2 g, 69.3 mmol), and the mixture was stirred at room temperature for 30 min. To the reaction solution was added monoethyl malonate magnesium salt (10 g, 34.8 mmol) and the mixture was stirred at room temperature for 2 hrs. To the reaction solution were added ethyl acetate (50 ml) and water (50 ml), and conc. hydrochloric acid was added until the pH of the aqueous layer became acidic. The reaction solution was extracted with ethyl acetate (200 ml×2). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give ethyl 3-oxo-3-(4-phenoxyphenyl)propionate (17.9 g, 100%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-c1aea9e0fce54cde85ead9f0ebb1c733
Source noteuspto-grants-2006_01