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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178301Generated: October 30, 2026

Potassium Carbonate → Tert-butyl 3-methoxy-4-((6-methoxypyridin-3-yl)methoxy)benzylcarbamate

https://huagongshe.com/reaction/2178301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 15713917HCID 15713917—
Reactant5-(Chloromethyl)-2-methoxypyridine hydrochlorideHCID 53438957—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 3-methoxy-4-((6-methoxypyridin-3-yl)methoxy)benzylcarbamateHCID 11811412496.2%

Reaction Steps

To a stirred solution of tert-butyl 4-hydroxy-3-methoxybenzylcarbamate (22.44 g, 88.59 mmol) in acetonitrile (250 mL) was added potassium carbonate (30.61 g, 221.5 mmol) and 5-(chloromethyl)-2-methoxypyridine hydrochloride (18.33 g, 94.46 mmol). The resulting mixture was heated to reflux and stirred. After 23 h, the light green suspension was allowed to cool to room temperature and was diluted with water (600 mL), resulting in the formation of a precipitate. The solids were isolated by filtration and washed with water. The moist solids were dissolved in dichloromethane (300 mL), and a small amount of water separated and was removed. The organic phase was dried over magnesium sulfate, filtered, and concentrated to provide 31.92 g (96%) of tert-butyl 3-methoxy-4-((6-methoxypyridin-3-yl)methoxy)benzylcarbamate as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067914B1
Source datasetuspto-grants-2015_06
ORD IDord-3acfe7501ca9470598f470eb681724c2
Source noteuspto-grants-2015_06