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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238397Generated: October 25, 2026

Ethyl 4-methoxyphenylacetate → Ethyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoate

https://huagongshe.com/reaction/238397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-methoxyphenylacetateHCID 84174—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-Cyano-2-methylbenzoyl chlorideHCID 86654215—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoateHCID 6717448888.7%

Reaction Steps

To a solution of (4-methoxy-phenyl)-acetic acid ethyl ester (25.96 g, 133.7 mmol) in anhydrous tetrahydrofuran (200 mL) was added lithium hexamethyldisilazide (200 mL, 1 M) at −78° C. under nitrogen. After being stirred for 15 min., a solution of A-5 (4-cyano-2-methylbenzoyl chloride) (24 g, 133.6 mmol) in anhydrous tetrahydrofuran (150 mL) was added dropwise, and the resulting mixture was stirred at room temperature overnight for 16 h. The reaction mixture was quenched by the addition of saturated aqueous ammonium chloride solution (200 mL), and the resultant mixture was extracted with ethyl acetate (100 mL×3). The combined organic layers were dried over anhydrous sodium sulfate (20 g), filtered, and evaporated. The residue was purified on silica gel column (petroleum ether/ethyl acetate=25:1) to give A-6 (ethyl 3-(4-cyano-2-methylphenyl)-2-(4-methoxyphenyl)-3-oxopropanoate) (40 g, yield 88.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642628B2
Source datasetuspto-grants-2014_02
ORD IDord-c636269a56a941f6a2caef914f6df5ff
Source noteuspto-grants-2014_02