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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606248Generated: October 25, 2026

Water → 2-[1-[4-(2-Fluorophenoxymethyl)piperidino]ethyl]-3-methoxypyrazine

https://huagongshe.com/reaction/606248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(3-Methoxy-2-pyrazinyl)ethanoneHCID 539832—
ReactantSodium borohydrideHCID 4311764—
Reactant4-[(2-Fluorophenoxy)methyl]piperidineHCID 17178051—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventTitanium isopropoxideHCID 11026—
Product2-[1-[4-(2-Fluorophenoxymethyl)piperidino]ethyl]-3-methoxypyrazineHCID 2224836511%

Reaction Steps

After dissolving 1.09 g of 4-(2-fluorophenoxymethyl)piperidine in 15 ml of methanol, 1.53 ml of titanium (IV) tetraisopropoxide and 400 mg of 2-acetyl-3-methoxypyrazine [CAS No. 56343-40-9] were added and the mixture was stirred overnight at room temperature. The reaction solution was cooled on ice, 148 mg of sodium borohydride was added and the mixture was stirred for 5 hours at room temperature. Water and ethyl acetate were added to the reaction solution and the mixture was filtered with celite. The filtrate was extracted with ethyl acetate and the extract was washed with saturated brine and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by NH silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (100 mg, 11% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915274B2
Source datasetuspto-grants-2011_03
ORD IDord-81cf126bcc0f4fd695df60207e1dba84
Source noteuspto-grants-2011_03