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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233295Generated: October 30, 2026

(Trifluoromethyl)trimethylsilane → HCID 59295451, compound

https://huagongshe.com/reaction/2233295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 59295400HCID 59295400—
ReactantHCID 59295476HCID 59295476—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59295451HCID 59295451—

Reaction Steps

To an ice cooled solution of 2.0 g 4-Methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazole-5-carbaldehyde (derived from [4-Methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazol-5-yl]-methanol according to the method described for 4-Methyl-2-(trans-1,4-trifluoromethyl-cyclohexyl)-thiazole-5-carbaldehyde) and 1.09 ml (trifluoromethyl)trimethylsilane in 10 ml tetrahydrofuran were added 100 mg tetrabutylammoniumfluoride. The reaction mixture was stirred at room temperature for thirty minutes. Then 20 ml 2N HCL were added and the mixture stirred at room temperature for thirty minutes. The mixture was extracted three times with portions of 50 ml ethyl acetate. The combined organic layers were dried over MgSO4. The solvent was evaporated in vacuo to obtain 1.5 g 2,2,2-Trifluoro-1-[4-methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazol-5-yl]-ethanol as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709481B2
Source datasetuspto-grants-2010_05
ORD IDord-6cb903c0da5d4eefa0d58a6e2d9ec3e3
Source noteuspto-grants-2010_05