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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(Trifluoroacetyl)imidazole | HCID 73767 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 1-(4-Bromo-3-(trifluoromethyl)phenyl)ethan-1-one | HCID 22313818 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[4-Bromo-3-(trifluoromethyl)phenyl]-4,4,4-trifluoro-1,3-butanedione | HCID 22313793 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06603008B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-ca68389d6ab54a068f87c43c238c72d8 |
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| Source note | uspto-grants-2003_08 |
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