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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706422Generated: October 31, 2026

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

https://huagongshe.com/reaction/706422

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 numberUS09174986B2
Source datasetuspto-grants-2015_11
ORD IDord-b781a7aef74b4e898f4fdf19798e50f5
Source noteuspto-grants-2015_11