Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
Reactant2-(1H-imidazol-1-yl)benzaldehydeHCID 10419625—
CatalystTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
Product2,2,2-Trifluoro-1-(2-imidazol-1-yl-phenyl)-ethanolHCID 6674279693%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968559B2
Source datasetuspto-grants-2011_06
ORD IDord-990f7394e67e48e4bfc9feab1487b282
Source noteuspto-grants-2011_06