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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224266Generated: November 1, 2026

2-Benzyl-4,5-dichloro-2,3-dihydropyridazin-3-one → 2-Benzyl-4-chloro-5-methoxypyridazin-3(2h)-one

https://huagongshe.com/reaction/2224266

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Benzyl-4,5-dichloro-2,3-dihydropyridazin-3-oneHCID 722438—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-Benzyl-4-chloro-5-methoxypyridazin-3(2h)-oneHCID 737015—

Reaction Steps

To a solution of 2-benzyl-4,5-dichloro-2H-pyridazine-3-one (22.31 g, 87.47 mmol), prepared as described in Example 244A, in dry MeOH (175 mL) at 0° C., was added dropwise a solution of sodium methoxide in methanol (25% weight in MeOH, 25 mL). The mixture was slowly warmed up to room temperature and stirred for 18 h. The reaction mixture was diluted with methylene chloride (200 mL) and filtered. The filtrate was concentrated to afford the title compound, 2-benzyl-4-chloro-5-methoxypyridazin-3(2H)-one (22.2 g) which was >95% pure as judged by HPLC and was used in the next reaction, Example 354B, without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378418B2
Source datasetuspto-grants-2008_05
ORD IDord-dc4920055d6943cfbcf8e8ea451d75fe
Source noteuspto-grants-2008_05