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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387804Generated: October 30, 2026

Ethyl Acetoacetate → Methyl 4-(2-(ethoxycarbonyl)-3-oxobutyl)-3-methoxybenzoate

https://huagongshe.com/reaction/2387804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(2-(ethoxycarbonyl)-3-oxobutyl)-3-methoxybenzoateHCID 66819542—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (60% in mineral oil; 1.45 g) was added portionwise over 10 min to a solution of ethyl acetoacetate (4.4 mL) in THF (60 mL) at 0° C. The resulting suspension was stirred at 0° C. for 10 min and a solution of methyl 4-(bromomethyl)-3-methoxybenzoate (7.5 g) in THF (40 mL) added portionwise over 10 min. The mixture was warmed to 70° C. and stirred for 15 h. The mixture was allowed to cool and then poured cautiously into ice/water (300 mL) and stirred for 30 min. The aqueous phase was extracted with EtOAc and the combined organic phase was dried filtered and evaporated to afford crude product. The reaction was repeated on an identical scale and the two batches of crude product were combined and purified by chromatography eluting with 20-30% EtOAc in isohexane to give the subtitle compound as a colorless oil 14.70 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268990B2
Source datasetuspto-grants-2012_09
ORD IDord-39ddeff2a8454c2eb234e102187f5345
Source noteuspto-grants-2012_09