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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913181Generated: October 26, 2026

Methyl iodide → 2-Chloro-5-(methoxymethyl)pyridine

https://huagongshe.com/reaction/1913181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant(6-Chloropyridin-3-yl)methanolHCID 177161—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-5-(methoxymethyl)pyridineHCID 19010921—

Reaction Steps

2.6 g (23.0 mmol) of potassium tert-butoxide are dissolved in 50 ml of THF. 3.0 g (20.9 mmol) of (6-chloropyridin-3-yl)methanol are added, and the mixture is stirred at RT for 15 min. 4.4 g (31.3 mmol) of iodomethane are then added slowly, and the mixture is stirred for about 30 min until the slightly exothermic reaction has subsided. The solvent is removed, and the residue is taken up in dichloromethane and washed twice with water. The organic phase is dried over magnesium sulfate and concentrated, and the residue is purified by column chromatography on silica gel (Biotage chromatography, mobile phase: cyclohexane/ethyl acetate 85:15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609698B2
Source datasetuspto-grants-2013_12
ORD IDord-6fb9a54992f846788acca02b8960c43c
Source noteuspto-grants-2013_12