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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625854Generated: November 2, 2026

Citric Acid → t-Butyl2-acetyl-4-(4-ethylphenyl)-3-oxobutyrate

https://huagongshe.com/reaction/1625854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantTert-butyl acetoacetateHCID 15538—
ReactantMagnesium ChlorideHCID 5360315—
Reactant4-Ethylphenylacetyl chlorideHCID 15578354—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Productt-Butyl2-acetyl-4-(4-ethylphenyl)-3-oxobutyrateHCID 66608203—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of magnesium chloride (1.74 g) in dichloromethane (30 ml) was cooled to 0° C., and thereto were added t-butyl acetoacetate (3.03 ml) and pyridine (2.96 ml), and successively was added a solution of the above 4-ethylphenylacetyl chloride in dichloromethane (30 ml). The mixture was stirred at the same temperature for 2.5 hours, and an aqueous citric acid solution was added thereto. The mixture was extracted with chloroform. The extract was washed with brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to give t-butyl 2-acetyl-4-(4-ethylphenyl)-3-oxobutyrate (4.75 g) as pale yellow oil. APCI-Mass m/Z 322 (M+NH4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-4915531292404465b1541f97a6d917a9
Source noteuspto-grants-2014_07