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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503230Generated: October 30, 2026

Ethyl Acetate → Ethyl 2-(3,4-dichlorobenzyl)-3-oxobutanoate

https://huagongshe.com/reaction/1503230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
Reactant4-(Bromomethyl)-1,2-dichlorobenzeneHCID 639726—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(3,4-dichlorobenzyl)-3-oxobutanoateHCID 67402529—

Reaction Steps

To a solution of ethyl acetoacetate (1.0 g) in tetrahydrofuran (20 mL) was added sodium hydride (about 60% oil suspension) (0.37 g) in several portions under ice-cooling under a nitrogen atmosphere. After stirring at room temperature for 1 hr, 3,4-dichlorobenzylbromide (1.4 mL) was added to the reaction mixture. After stirring at room temperature for 2 hr, the reaction mixture was poured into a mixture of ethyl acetate and water. The organic phase was washed successively with water and brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by column chromatography on silica gel by eluting with toluene. An eluted fraction containing the desired product was recovered and evaporated under reduced pressure to give ethyl 2-acetyl-3-(3,4-dichlorophenyl)propanoate (35) (1.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212169B2
Source datasetuspto-grants-2015_12
ORD IDord-95f5cc8ad77446eda9277125689b4636
Source noteuspto-grants-2015_12