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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640899Generated: October 31, 2026

Chloromethyl Methyl Ether → 2-chloro-5-(MethoxyMethoxy)pyridine

https://huagongshe.com/reaction/1640899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-5-hydroxypyridineHCID 819821—
SolventWaterHCID 962—
SolventSodium ChlorideHCID 5234—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-chloro-5-(MethoxyMethoxy)pyridineHCID 5876419381%

Reaction Steps

Suspend sodium hydride (3.7 g, 93 mmol) in DMF (50 mL) and add a solution of 2-chloro-5-hydroxypyridine (10 g, 77 mmol) in DMF (20 mL) dropwise over 45 min. Stir the resulting solution at RT for 1.5 h. Add chloromethylmethyl ether (6.6 mL, 86 mmol) dropwise over 45 min. Stir the resulting mixture at RT for 12 h. Dilute the mixture with ethyl acetate, water, and saturated aqueous sodium chloride. Isolate the organic solution and wash with three portions of water, one portion of saturated aqueous sodium chloride, dry over sodium sulfate, filter, and concentrate in vacuo. Purify the crude product by column chromatography on 330 g of silica gel eluting with a gradient from hexane to 30% ethyl acetate in hexane over 20 min and then hold at 30% ethyl acetate in hexane for 30 min to give the title compound 10.8 g (81%) as a clear oil. MS (ES) m/z 174.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114872B2
Source datasetuspto-grants-2012_02
ORD IDord-ebac8bc3254c4a16ba8538215c7b9902
Source noteuspto-grants-2012_02