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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455554Generated: November 2, 2026

Chloromethyl Methyl Ether → 6-Chloro-2-fluoro-3-(methoxymethoxy)pyridine

https://huagongshe.com/reaction/455554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-2-fluoropyridin-3-olHCID 57475640—
SolventAcetoneHCID 180—
Product6-Chloro-2-fluoro-3-(methoxymethoxy)pyridineHCID 5747564182.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 6-chloro-2-fluoropyridin-3-ol (1.4 Kg, 9.49 mol) was dissolved in acetone (13 L), and treated with K2CO3 (1574 g, 11.39 mol, 1.2 eq) and MOMCl (840 g, 10.44 mol, 1.1 eq). The mixture was heated at 60° C. for 2 hrs. After cooling to RT, the reaction mixture was filtered to remove inorganic salts. The filtrate was concentrated under reduced pressure. The residue was purified by flash column chromatography (0-10% EtOAc/hexanes), affording 6-chloro-2-fluoro-3-(methoxymethoxy)pyridine (1496 g) as a colorless oil in 80% yield over two steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497264B2
Source datasetuspto-grants-2013_07
ORD IDord-24d77b97b9ac422cb61dc1b27eddc73e
Source noteuspto-grants-2013_07