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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597484Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/1597484

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, 1.2 mmol) 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 to the 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 numberUS06294558B1
Source datasetuspto-grants-2001_09
ORD IDord-dd99a2f70be241dfb12ab52cfb0b765d
Source noteuspto-grants-2001_09