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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005375Generated: October 30, 2026

Water → 3-(methoxymethyl)pyridine

https://huagongshe.com/reaction/1005375

Reaction equation

Participants

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

Reaction Steps

A solution of 3-hydroxymethylpyridine (10 g, 92 mmol) in anhydrous tetrahydrofuran (200 ml), under an atmosphere of nitrogen, was treated with sodium hydride (4 g of a 55% oil dispersion, 92 mmol) in portions. After stirring for 15 minutes iodomethane (5.7 ml, 92 mmol) was added dropwise and the reaction mixture was stirred at ambient temperature for 2 hours. Water (20 ml) was added and the tetrahydrofuran evaporated. The residue was partitioned between water (50 ml) and dichloromethane (70 ml). The organic layer was separated, dried (sodium sulphate) then evaporated. The crude product was purified by column chromatography on silica using ethyl acetate. The title compound was obtained (11 g, 93%) as an oil, δH (250 MHz, CDCl3) 3.42 (3H, s), 4.48 (2H, s), 7.27-7.32 (1H, m), 7.66-7.71 (1H, m), 8.53-8.60 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054469
Source datasetuspto-grants-2000_04
ORD IDord-851e06dd801c4fc3807b95b8707281b1
Source noteuspto-grants-2000_04