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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211589Generated: November 4, 2026

Ethyl Acetoacetate → Ethyl 3-(4-methylphenyl)-3-oxopropanoate

https://huagongshe.com/reaction/2211589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
Reactant4-Methylbenzoyl ChlorideHCID 13405—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductEthyl 3-(4-methylphenyl)-3-oxopropanoateHCID 29263735%

Reaction Steps

Sodium hydroxide solution (33%, 32.5 ml) was added to ethyl acetoacetate (97.5 g, 750 mmol) in a mixture of water (250 ml) and toluene (12 ml) at 0–5° C. under stirring (pH 11). After 30 minutes 4-methylbenzoylchloride (127.46 g, 825 mmol) and sodium hydroxide solution (33%, 135 ml) was added simultaneously over a period two hours. The reaction mixture was stirred for 15 minutes at 0° C. and for 1 hour at 35° C. Aqueous layer was separated, ammonium chloride (40 g) was added and stirred slowly over night. The reaction mixture was saturated with sodium chloride and extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over anhydrous sodium sulphate and concentrated to dryness in vacuum. The crude product thus obtained was purified by column chromatography to yield the title compound as viscous oil (54 g, 35%). MS m/z: 207.1 (M+). Preparation 2 Synthesis of ethyl(4-chloro)benzoylacetate

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101873B2
Source datasetuspto-grants-2006_09
ORD IDord-a10cd8a4411a4f5586cd7b0d650cc384
Source noteuspto-grants-2006_09