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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446892Generated: October 26, 2026

Chloromethyl Methyl Ether → 4,5-dichloro-2-methoxymethyl-2H-pyridazin-3-one

https://huagongshe.com/reaction/446892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
Reactant4,5-Dichloro-3-hydroxypyridazineHCID 73247—
ReactantDiisopropylethylamineHCID 81531—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4,5-dichloro-2-methoxymethyl-2H-pyridazin-3-oneHCID 12351834583.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

4,5-Dichloro-2H-pyridazin-3-one (30 g, 182 mmol), N,N-diisopropylethylamine (47.5 mL, 258 mmol) and 4-dimethylaminopyridine (2.20 g, 18.2 mmol) were dissolved in 200 mL of methylene chloride, to which was slowly added dropwise chloromethyl methyl ether (16.6 mL, 21.8 mmol) while maintaining at 0° C. The mixture was stirred for 3 h at room temperature. The reaction solution was washed with saturated aqueous sodium hydrogen carbonate solution, distilled under reduced pressure, and separated-purified by column chromatography (10% methylene chloride/ethyl acetate) to give the title compound (26.6 g, Yield: 70%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481537B2
Source datasetuspto-grants-2013_07
ORD IDord-1e8a5b17c8074463a49096be65b85ec9
Source noteuspto-grants-2013_07