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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507294Generated: October 30, 2026

Ethyl Acetate → HCID 86715647, compound

https://huagongshe.com/reaction/1507294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-oxovalerateHCID 78656—
Reactant1-(Bromomethyl)-4-(trifluoromethyl)benzeneHCID 123062—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86715647HCID 86715647—

Reaction Steps

Sodium hydride (60% dispersion in mineral oil, 1.75 g, 43.7 mmol) was added in portions over 1 minute to an ice-cooled, stirring solution of ethyl 3-oxopentanoate (6.30 g, 43.7 mmol) in dry dimethoxyethane (87 mL). After 5 minutes, the flask was removed from the cooling bath and stirring continued at room temperature. After 30 minutes, a solution of 4-(trifluoromethyl)benzyl bromide (10.4 g, 43.7 mmol) in dry dimethoxyethane (10 mL) was added dropwise over 2 minutes. After 2.5 hours, ethyl acetate (300 mL) and water (100 mL) were added. The layers were separated. The organic layer was dried with sodium sulfate and the dried solution was filtered. The filtrate was concentrated and the residue was purified by flash-column chromatography on silica gel eluting with hexanes initially, grading to 50% dichloromethane-hexanes to provide the title compound as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221804B2
Source datasetuspto-grants-2015_12
ORD IDord-013fe9b6323c42cd9203ed133617b5b0
Source noteuspto-grants-2015_12