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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207285Generated: October 31, 2026

Chloromethyl Methyl Ether → 2-chloro-5-(MethoxyMethoxy)pyridine

https://huagongshe.com/reaction/2207285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-5-hydroxypyridineHCID 819821—
SolventDimethylformamideHCID 6228—
Product2-chloro-5-(MethoxyMethoxy)pyridineHCID 58764193—

Reaction Steps

1000 mg (1 eq) of 6-chloropyridin-3-ol was dissolved in 50 mL of N,N-dimethylformamide, and 370 mg (1.2 eq) of sodium hydride was added thereto, followed by stirring at room temperature for 1 hour. Then, 688 uL (1.1 eq) of chloro(methoxy)methane was added slowly thereto, and the solution was stirred at room temperature for 2 hours. N,N-dimethylformamide was removed by concentrating under reduced pressure. After extracting with ethyl acetate, the extract was treated with anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was separated by column chromatography (developing solvent, hexane:ethyl acetate=9:1) to obtain 1200 mg of 2-chloro-5-(methoxymethoxy)pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376429B2
Source datasetuspto-grants-2016_06
ORD IDord-658069f554704a9486a742f4964dbd22
Source noteuspto-grants-2016_06