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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055636Generated: November 2, 2026

Tetrabutylammonium Fluoride → [1-(4-fluoro-phenyl)-2-methyl-1H-imidazol-4-yl]-methanol

https://huagongshe.com/reaction/2055636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-(tert-butyl-dimethyl-silanyloxymethyl)-1-(4-fluoro-phenyl)-2-methyl-1H-imidazoleHCID 131726173—
SolventTetrahydrofuranHCID 8028—
Product[1-(4-fluoro-phenyl)-2-methyl-1H-imidazol-4-yl]-methanolHCID 67303957—

Reaction Steps

4-(tert-Butyl-dimethyl-silanyloxymethyl)-1-(4-fluoro-phenyl)-2-methyl-1H-imidazole (14.7 g, 45.7 mmol) was dissolved in 200 mL THF. Tetrabutyl ammoniumfluoride (91 mL, 1M in THF, 91 mmol) was added and the reaction mixture was stirred at room temperature overnight. The solvent was evaporated. The residue was taken up in 200 mL water and extracted three times with ethyl acetate (200 mL each). The combined organic extracts were dried with magnesium sulfate, filtered and evaporated. The crude product was suspended in 150 mL ethyl acetate, filtered and dried. The desired compound was obtained as a white solid (7.16 g, 76%), MS: m/e=207.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332510B2
Source datasetuspto-grants-2008_02
ORD IDord-c412a28b0f954cdf8781f86b40d628f1
Source noteuspto-grants-2008_02