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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599859Generated: October 31, 2026

Tetrabutylammonium Fluoride → [2-(Benzhydrylidene-amino)-3-fluoropyridin-4-yl]-methanol

https://huagongshe.com/reaction/599859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantBenzhydrylidene-[4-(tert-butyldimethylsilyloxymethyl)-3-fluoropyridin-2-yl]-amineHCID 59139248—
SolventEthyl AcetateHCID 8857—
Product[2-(Benzhydrylidene-amino)-3-fluoropyridin-4-yl]-methanolHCID 59139234—

Reaction Steps

A mixture of benzhydrylidene-[4-(tert-butyldimethylsilyloxymethyl)-3-fluoropyridin-2-yl]-amine (14 mg, 32 μmol) and tetrabutylammonium fluoride (1 mol/L in THF) (65 μL, 65 μmol) in THE (0.5 mL) was stirred at room temperature for 30 minutes. Ethyl acetate was then added to the reaction solution, and the solution was washed with sodium hydrogen carbonate solution and saturated saline. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled away under reduced pressure. The resultant residue was purified by silica gel column chromatography to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897792B2
Source datasetuspto-grants-2011_03
ORD IDord-0da9b75b44e5436190e2482b6dbdb79d
Source noteuspto-grants-2011_03