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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473353Generated: October 30, 2026

Chloromethyl Methyl Ether → 3-(Methoxymethoxy)pyridine

https://huagongshe.com/reaction/473353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
Reactant3-HydroxypyridineHCID 7971—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product3-(Methoxymethoxy)pyridineHCID 375439727.6%

Reaction Steps

Pyridin-3-ol (25 g, 260 mmol) was added to a stirring mixture of NaH (11 g of a 60 wt % dispersion with mineral oil, 260 mmol) and DMF (350 mL) at 0° C. After 30 min, the reaction mixture was allowed to warm to RT, stirred for 90 min, and then chloromethoxymethane (20 mL, 260 mmol) was added. After 18 h, the reaction mixture was partitioned between ethyl acetate and saturated aqueous NaHCO3. The layers were separated, the organic material was washed with saturated aqueous NaHCO3, brine, dried (Na2SO4), filtered, and the filtrate was concentrated. The residue was dissolved with CH2Cl2, the solution was filtered through a plug of silica gel (sequential elution; 9:1-1:1 hexane-ethyl acetate), and the second filtrate was concentrated to give 10 g (27%) of 3-(methoxymethoxy)pyridine as a clear yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633315B2
Source datasetuspto-grants-2014_01
ORD IDord-c976a833992548ac95e8fc9023b28ed2
Source noteuspto-grants-2014_01