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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224277Generated: November 1, 2026

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

https://huagongshe.com/reaction/2224277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Benzyl-4,5-dichloro-2,3-dihydropyridazin-3-oneHCID 722438—
ReactantSodium MethoxideHCID 10942334—
Solvent1,4-DioxaneHCID 31275—
Product2-Benzyl-5-chloro-4-methoxypyridazin-3(2H)-oneHCID 1352621390.2%

Reaction Steps

To a stirring solution of 2-benzyl-4,5-dichloropyridazin-3(2H)-one (22.9 g, 89.8 mmol) in 1,4-dioxane (300 mL) at RT under argon was added NaOMe (22.4 mL, 25% solution in MeOH, 97.9 mmol) over 10 min by syringe. After 2 h, TLC indicated the reaction was completed. The reaction mixture was concentrated under reduced pressure. A saturated solution of NaCl (200 mL) was added and the resulting solution was extracted with CH2Cl2 (2×100 mL). The combined organic layers were dried (Na2SO4), concentrated under vacuum and purified by silica gel column chromatography eluting with CH2Cl2 to give the title compound, 2-benzyl-5-chloro-4-methoxypyridazin-3(2H)-one (20.3 g, 90%) as a colorless oil. TLC (CH2Cl2, Rf=0.4); MS [M+H]+ 251; HPLC retention time=2.74 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378418B2
Source datasetuspto-grants-2008_05
ORD IDord-a70da90f2d4f409fad8a7c7f11105a53
Source noteuspto-grants-2008_05