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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2094498Generated: October 30, 2026

Methyl iodide → 3-(methoxymethyl)pyridine

https://huagongshe.com/reaction/2094498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant3-PyridinemethanolHCID 7510—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
Product3-(methoxymethyl)pyridineHCID 338926—

Reaction Steps

To a mixture of 10.0 g of 3-hydroxymethylpyridine and 200 ml of THF, 3.7 g of 60% sodium hydride (in oil) was added in small portions at room temperature and then stirred for 15 minutes. To the reaction mixture, 13.0 g of methyl iodide was added dropwise, and the reaction mixture was stirred at room temperature for three hours. To the reaction mixture, 25 ml of water was added. Then, the reaction mixture was concentrated under reduced pressure. To the residue, 25 ml of water was added, followed by extraction with ethyl acetate three times. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 8.17 g of 3-methoxymethylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445522B2
Source datasetuspto-grants-2013_05
ORD IDord-b0044186d97e40ac8a6d5d9864845bfa
Source noteuspto-grants-2013_05