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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246187Generated: November 2, 2026

Methyl iodide → 2-Chloro-3-methoxypyridine

https://huagongshe.com/reaction/2246187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-Chloro-3-pyridinolHCID 81136—
ReactantSodium MethoxideHCID 10942334—
SolventDimethylformamideHCID 6228—
Product2-Chloro-3-methoxypyridineHCID 10425246.9%

Reaction Steps

To a solution of 2-chloro-3-hydroxypyridine (25 g; 193 mmol) in N,N-dimethylformamide (250 mL) was added sodium methoxide (11.5 g; 212 mmol). The mixture was stirred for 4 hours at room temperature and methyl iodide (24 mL; 386 mmol) was added. The resulting mixture was stirred for another 16 hours. The reaction mixture was quenched with water and extracted with dichloromethane. The combined extracts were washed with water, dried over sodium sulfate and concentrated under reduced pressure to provide product (13 g) as a yellow oil. The aforementioned product, 2-chloro-3-methoxypyridine (2), was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687487B2
Source datasetuspto-grants-2010_03
ORD IDord-4cb59668f4fc48fdb7c80a6cd202df4c
Source noteuspto-grants-2010_03