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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422097Generated: October 30, 2026

Chloromethyl Methyl Ether → 3-(Methoxymethoxy)pyridine

https://huagongshe.com/reaction/422097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
Reactant3-HydroxypyridineHCID 7971—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product3-(Methoxymethoxy)pyridineHCID 3754397—

Reaction Conditions

Temperature-15 °C

Reaction Steps

Dissolve 3-hydroxypyridine (7 g, 74 mmol) in THF (20.6 mL) and dimethylformamide (34.4 mL) and cool to −15° C. Add potassium tert-butoxide (8.3 g, 74 mmol) and stir at −15° C. for 30 min. Treat the mixture with chloromethylmethyl ether (5.81 mL, 77 mmol) dropwise over 40 min. After the addition is complete, stir the mixture at −15° C. for an additional hour. Remove the ice bath and allow the mixture to warm slowly to 15° C. Pour the mixture into saturated aqueous sodium chloride and stir vigorously for 10 min. Extract the resulting solution with three portions of ethyl acetate. Combine the organic extracts and wash with saturated aqueous sodium chloride, dry over sodium sulfate, filter, and concentrate in vacuo. Use the resulting product without further purification. 1H NMR (400 MHz, CDCl3) δ 8.42 (d, J=3 Hz, 1H), 8.28 (d, J=5 Hz, 1H), 7.37-7.42 (m, 1H), 7.21-7.27 (m, 1H), 5.20 (s, 2H), 3.49 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101628B2
Source datasetuspto-grants-2012_01
ORD IDord-13dd34ce70fd4bdbb936abb47899fdef
Source noteuspto-grants-2012_01