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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821655Generated: November 1, 2026

Sodium Methoxide → 6-Chloro-4-methoxy-3-(2-methylphenoxy)pyridazine

https://huagongshe.com/reaction/1821655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 23013971HCID 23013971—
SolventMethanolHCID 887—
Product6-Chloro-4-methoxy-3-(2-methylphenoxy)pyridazineHCID 2294013693.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

In methanol (60 mL) was dissolved 3.00 g (11.8 mmol) of 4,6-dichloro-3-(2-methylphenoxy)pyridazine obtained in Example 1 (2), 1.00 g (17.6 mmol) of 95% sodium methoxide was added to the solution at room temperature and the mixture was stirred at 60° C. for 4 hours. Moreover, 1.00 g (17.6 mmol) of 95% sodium methoxide was further added and after stirring the mixture at 60° C. for 1 hour, it was allowed to stand at room temperature overnight. The reaction mixture was concentrated, ethyl acetate was added to the residue, and the mixture was successively washed with water and brine. After drying over anhydrous sodium sulfate, the solvent was removed, and the obtained residue was purified by silica gel column chromatography (eluted with hexane:ethyl acetate=4:1) to obtain 2.75 g (11.0 mmol, Yield: 93.2%) of 6-chloro-4-methoxy-3-(2-methylphenoxy)pyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608563B2
Source datasetuspto-grants-2009_10
ORD IDord-aaf59902ab854be0935424559dfe831f
Source noteuspto-grants-2009_10