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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021306Generated: November 3, 2026

Water → HCID 68310301, compound

https://huagongshe.com/reaction/1021306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl methyl etherHCID 80972—
Reactant4-{4-[2-fluoro-3-(hydroxymethyl)phenyl]piperazin-1-yl}pyridin-2(1H)-oneHCID 68309869—
CatalystTetrabutylammonium IodideHCID 67553—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 68310301HCID 6831030129.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-{4-[2-Fluoro-3-(hydroxymethyl)phenyl]piperazin-1-yl}pyridin-2(1H)-one (300 mg) was suspended in DMF (7.5 ml), and potassium carbonate (273 mg), 2-bromoethylmethyl ether (275 mg), and tetrabutylammonium iodide (37 mg) were added thereto, followed by stirring at 60° C. overnight. Water and CHCl3 were added to the reaction mixture, and the organic layer was washed with saturated brine and then dried over Na2SO4. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (MeOH/CHCl3) to obtain (2-fluoro-3-{4-[2-(2-methoxyethoxy)pyridin-4-yl]piperazin-1-yl}phenyl)methanol (104 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-1eb1d74780d14abd822982991e78c6b9
Source noteuspto-grants-2014_05