Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884582Generated: October 31, 2026

Methyl iodide → 2-Phenoxy-3-[3-(3-methoxypyridin-4-yl)propoxy]pyridine

https://huagongshe.com/reaction/1884582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant2-Phenoxy-3-[3-(3-hydroxypyridin-4-yl)propoxy]pyridineHCID 9883625—
SolventDimethylformamideHCID 6228—
Product2-Phenoxy-3-[3-(3-methoxypyridin-4-yl)propoxy]pyridineHCID 23506246—

Reaction Steps

Sodium hydride (60% in mineral oil, 0.04 g, 1.0 mmol) is suspended in DMF (10 ml), and thereto is added 2-phenoxy-3-[3-(3-hydroxypyridin-4-yl)propoxy]pyridine (0.20 g, 0.62 mmo) obtained in Example 30 at room temperature, and the mixture is stirred for 30 minutes. To the mixture is added methyl iodide (0.06 ml, 1.0 mmol) under ice-cooling, and the mixture is stirred for 1 0 minutes. To the reaction solution is added ethyl acetate (50 ml), and the mixture is washed with a saturated brine (30 ml×2), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: chloroform/methanol), and recrystallized from isopropyl ether to give the title compound (0.09 g) as colorless crystals, m.p. 101-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06765095B2
Source datasetuspto-grants-2004_07
ORD IDord-872547a17a1842209acd55cdea9d5557
Source noteuspto-grants-2004_07