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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221843Generated: October 26, 2026

Ethyl bromoacetate → 4-(4-Methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl ester

https://huagongshe.com/reaction/221843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant4-PropanoylanisoleHCID 67144—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl esterHCID 14866576125.6%

Reaction Steps

A solution of 4-methoxypropiophenone (24 g, 140 mmol) in tetrahydrofuran (220 mL) was cooled to 0° C. Lithium diisopropylamide, (2M solution in THF) (126 mL, 248 mmol) was added dropwise and warmed to rt for 30 min. The reaction was cooled again to 0° C. and ethyl bromoacetate (18 mL, 161 mmol) was added dropwise and warmed to rt for 30 min and then quenched with aqueous 1M HCl acid at 0° C. The aqueous layer was extracted twice with methylene chloride and the combined organics were washed with brine, dried (Na2SO4), filtered, and concentrated to give 4-(4-methoxyphenyl)-3-methyl-4-oxobutyric acid ethyl ester (44 g), MS m/z 205 (M−45).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207168B2
Source datasetuspto-grants-2012_06
ORD IDord-f7e3fa5d531c43d2a61a44b30b9655c7
Source noteuspto-grants-2012_06