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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620838Generated: November 1, 2026

(Trifluoromethyl)trimethylsilane → HCID 66743460, compound

https://huagongshe.com/reaction/1620838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
Reactant2-Pyrazol-1-yl-benzaldehydeHCID 965866—
CatalystTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66743460HCID 6674346093%

Reaction Steps

To 2-pyrazol-1-yl-benzaldehyde (0.344 g, 2 mmol) in THF (8 ml) was added trifluoromethyl trimethyl silane (0.341 g, 2.4 mmol). The 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 h. 2N HCl (5 ml) was added and the reaction mixture was further stirred at room temperature for 3 h. Solvent was removed on the rotavap under reduced pressure. The residue was dissolved in DCM (30 ml), washed with water (20 ml), brine (20 ml) and dried over sodium sulfate. The solvent was removed in vacuo to give crude 2,2,2-trifluoro-1-(2-pyrazol-1-yl-phenyl)-ethanol (0.45 g, 93%) which was directly used in the following experiment.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772482B2
Source datasetuspto-grants-2014_07
ORD IDord-3755a5be8c2b4733851d12b9d334f135
Source noteuspto-grants-2014_07