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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394866Generated: October 25, 2026

1-(Trifluoroacetyl)imidazole → 1-[4-Bromo-3-(trifluoromethyl)phenyl]-4,4,4-trifluoro-1,3-butanedione

https://huagongshe.com/reaction/394866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Trifluoroacetyl)imidazoleHCID 73767—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(4-Bromo-3-(trifluoromethyl)phenyl)ethan-1-oneHCID 22313818—
SolventTetrahydrofuranHCID 8028—
Product1-[4-Bromo-3-(trifluoromethyl)phenyl]-4,4,4-trifluoro-1,3-butanedioneHCID 2231379388%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-[4-bromo-3-(trifluoromethyl)phenyl]-1-ethanone (1.34 g, 5.65 mmol) in THF (30 ml) was added lithium bis(trimethylsilyl)amide (1.0 M THF solution, 6.8 ml, 6.8 mmol) at −78° C. The mixture was stirred at 0° C. for 15 minutes and the solution was again cooled to −78° C. N-trifluoroacetylimidazole (1.15 g, 6.78 mmol) was added to the solution at the same temperature. The resulting mixture was stirred at −78° C. for 15 minutes and at room temperature for 2.5 hours. The reaction was quenched with 2N HCl (100 ml). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (100 ml×2). The combined organic layer was washed with brine (200 ml), dried over MgSO4, and concentrated in vacuo to give 1.80 g (88%) of the title compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06603008B1
Source datasetuspto-grants-2003_08
ORD IDord-ca68389d6ab54a068f87c43c238c72d8
Source noteuspto-grants-2003_08