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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178401Generated: October 30, 2026

Potassium Carbonate → Tert-butyl 4-((6-(difluoromethyl)pyridin-3-yl)methoxy)-3-methoxybenzylcarbamate

https://huagongshe.com/reaction/2178401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 15713917HCID 15713917—
Reactant5-(Chloromethyl)-2-(difluoromethyl)pyridine hydrochlorideHCID 118113963—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 4-((6-(difluoromethyl)pyridin-3-yl)methoxy)-3-methoxybenzylcarbamateHCID 118114378105.7%

Reaction Steps

To a stirred solution of tert-butyl 4-hydroxy-3-methoxybenzylcarbamate (4.70 g, 18.56 mmol) and potassium carbonate (7.64 g, 55.28 mmol) in acetonitrile (50 mL) was added 5-(chloromethyl)-2-(difluoromethyl)pyridine hydrochloride (4.58 g, 21.40 mmol). The mixture was heated to reflux. After 3 h, the off-white suspension was allowed to cool to room temperature and was diluted with water (200 mL). The mixture was extracted with dichloromethane (3×75 mL). The combined organic phases were dried over magnesium sulfate, filtered, and concentrated to provide 7.74 g (>100%) of tert-butyl 4-((6-(difluoromethyl)pyridin-3-yl)methoxy)-3-methoxybenzylcarbamate as a waxy yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067914B1
Source datasetuspto-grants-2015_06
ORD IDord-694a1eca06d548deaf37812dbd66b7c6
Source noteuspto-grants-2015_06