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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224268Generated: November 1, 2026

Aluminum(III) Chloride → 4-chloro-5-(4-chlorophenyl)-2H-pyridazin-3-one

https://huagongshe.com/reaction/2224268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-benzyl-4-chloro-5-(4-chlorophenyl)pyridazin-3(2H)-oneHCID 59716654—
SolventTolueneHCID 1140—
Product4-chloro-5-(4-chlorophenyl)-2H-pyridazin-3-oneHCID 59716780100.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

2-Benzyl-4-Chloro-5-(4-chloro-phenyl)-2H-pyridazin-3-one (3.19 g, 9.65 mmol) was dissolved in toluene (50 mL). Aluminum chloride (AlCl3, 3.22 g, 24.1 mmol) was then added and the reaction mixture was heated at 50° C. After 20 min, the reaction mixture was cooled to RT and then poured into ice-water (200 mL). The resultant solution was extracted with EtOAc (3×200 mL). The combined organic layers were washed with water (500 mL). The organic layer was dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using EtOAc to give the title compound, 4-chloro-5-(4-chlorophenyl)-2H-pyridazin-3-one (2.33 g) as a white solid. HPLC: 2.74 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378418B2
Source datasetuspto-grants-2008_05
ORD IDord-ff69ac71302b43918854a342e1e2632e
Source noteuspto-grants-2008_05