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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396737Generated: October 25, 2026

Ethyl trifluoroacetate → Butane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-

https://huagongshe.com/reaction/396737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
ReactantHexamethyldisilazaneHCID 13838—
Reactant1-(4-(1H-Imidazol-1-yl)phenyl)ethanoneHCID 82316—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductButane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-HCID 6426099—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a THF (5 mL) solution of 1,1,1,3,3,3-hexamethyldisilazane (0.178 g, 1.1 mmol) was added n-butyl lithum (1.6 M solution in hexane, 0.72 mL, 1.2mmol) at 0° C. under nitrogen, and the mixture was stirred for 30 minutes, and cooled to −78° C. 4-(1-Imidazolyl)acetophenone (prepared according the method of M. A. Khan et, al., J. Chem. Soc. C., 1970, 85., 0.186 g, 1.0 mmol) was added to the mixture, and residue was stirred for 1 hour. Ethyl trifluoroacetate (0.17 g, 1.2 mmol) was added tothe reaction mixture, the residure was warm to room temperature. The reaction mixture was poured into ice water and the whole was extracted with ethyl acetate (30 mL×2). The organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The resulting solid was washed with small amount of ethyl acetate to give the title compound (0.163 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608095B2
Source datasetuspto-grants-2003_08
ORD IDord-014edeebc2ec4087a1b941830e15dd7f
Source noteuspto-grants-2003_08