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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837695Generated: November 4, 2026

Water → 1-[(2-Methoxy-3-pyridyl)methyl]-4-piperidineethanol

https://huagongshe.com/reaction/1837695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-PiperidineethanolHCID 73953—
Reactant3-(Chloromethyl)-2-methoxypyridineHCID 14932945—
SolventDimethylformamideHCID 6228—
Product1-[(2-Methoxy-3-pyridyl)methyl]-4-piperidineethanolHCID 22678724—

Reaction Steps

8.2 g of 4-piperidineethanol, 10.0 g of 3-(chloromethyl)-2-methoxypyridine and 17.5 g of potassium carbonate were suspended in 65 ml of N,N-dimethylformamide, and the mixture was stirred at room temperature for 12 hours. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, to give the title compound as a yellow oil (quantitatively).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784192B2
Source datasetuspto-grants-2004_08
ORD IDord-2ab587820f6e4d3da10ff5fa436e751f
Source noteuspto-grants-2004_08