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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387813Generated: October 30, 2026

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

https://huagongshe.com/reaction/2387813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-(bromomethyl)-3-fluorobenzoateHCID 18766370—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(2-(ethoxycarbonyl)-3-oxobutyl)-3-fluorobenzoateHCID 68412608—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (60% dispersion in mineral oil; 2.45 g) was added portionwise over 10 min to a solution of ethyl acetoacetate (7.5 mL) in THF (60 mL) at 0° C. under nitrogen. The resulting mixture was stirred at 0° C. for 10 min and a solution of methyl 4-(bromomethyl)-3-fluorobenzoate (12.1 g) in THF (40 mL) added over 10 min. The mixture was heated to 65° C. for 15 h and allowed to cool. The mixture was poured cautiously into ice/water (300 mL) and the aqueous extracted with EtOAc. The combined organic phase was dried, filtered and evaporated. The crude product was purified by chromatography eluting with 10 to 20% EtOAc in isohexane to give the subtitle compound as a colorless oil 110.10 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268990B2
Source datasetuspto-grants-2012_09
ORD IDord-6518e68aec3148c9a54e92417e21f6ed
Source noteuspto-grants-2012_09