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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046813Generated: October 29, 2026

Ethyl Acetate → [2-(Benzhydrylidene-amino)-3-fluoropyridin-4-yl]-methanol

https://huagongshe.com/reaction/1046813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantBenzhydrylidene-[4-(tert-butyldimethylsilyloxymethyl)-3-fluoropyridin-2-yl]-amineHCID 59139248—
SolventTetrahydrofuranHCID 8028—
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 THF (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 numberUS08569378B2
Source datasetuspto-grants-2013_10
ORD IDord-09a60985dfd949358b985696418b7540
Source noteuspto-grants-2013_10