HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426401Generated: October 31, 2026
(Trifluoromethyl)trimethylsilane → 2,2,2-Trifluoro-1-(2-imidazol-1-yl-phenyl)-ethanol
https://huagongshe.com/reaction/2426401
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | 2-(1H-imidazol-1-yl)benzaldehyde | HCID 10419625 | — |
| Catalyst | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2,2-Trifluoro-1-(2-imidazol-1-yl-phenyl)-ethanol | HCID 66742796 | 93% |
Reaction Steps
To 2-imidazol-1-yl-benzaldehyde (0.344 g, 2 mmol) in THF (8 ml) was added trifluoromethyltrimethyl silane (0.341 g, 2.4 mmol). The reaction mixture was cooled to 0-5° C. (ice water bath) and tetra-n-butyl ammonium fluoride (0.035 ml, 0.035 mmol, 1M in THF) was added. The ice bath was removed, and the mixture was stirred at room temperature for 6 hours. 2N HCl (5 ml) was added, and the reaction mixture was further stirred for 3 hours at room temperature. Solvent was removed on the rotavap under reduced pressure. Crude residue was dissolved in DCM (30 ml), washed with water (20 ml), brine (20 ml) and dried with sodium sulfate. The solvent was removed to give crude 2,2,2-trifluoro-1-(2-imidazol-1-yl-phenyl)-ethanol (0.45 g, 93%), which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968559B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-990f7394e67e48e4bfc9feab1487b282 |
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| Source note | uspto-grants-2011_06 |
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