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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224237Generated: October 31, 2026

Phosphorus oxychloride → 2-benzyl-4-chloro-5-(4-chlorophenyl)pyridazin-3(2H)-one

https://huagongshe.com/reaction/2224237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-benzyl-5-(4-chlorophenyl)-4-methoxypyridazin-3(2H)-oneHCID 56927522—
SolventMethanolHCID 887—
Product2-benzyl-4-chloro-5-(4-chlorophenyl)pyridazin-3(2H)-oneHCID 5971665466%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 2-benzyl-5-(4-chlorophenyl)-4-methoxypyridazin-3(2H)-one (13.8 g, 42.23 mmol) and POCl3 (20.0 mL) was stirred at 75° C. for 4 h. The reaction mixture was cooled to RT and concentrated under reduced pressure. The residue was cooled in an ice bath and water (200 mL) was added. The undissolved material was filtered and washed with water (3×150 mL). To the solid thus obtained was added MeOH (100 mL). The resultant mixture was sonicated for 10 mins, and then was filtered. The collected solid was washed with MeOH (2×50 mL). The solid was then dried in an vacuum oven at 50° C. to give the title compound, 2-benzyl-4-chloro-5-(4-chlorophenyl)pyridazin-3(2H)-one, (9.2 g, 66%) as a light brown solid. HPLC: 3.75 min; M+H=331. 1H NMR (CDCl3, 500 MHz): δ 7.73 (1H, s), 7.50 (2H, d, J=10.0 Hz), 7.47 (2H, d, J=10.0 Hz), 7.42 (2H, d, J=10.0 Hz), 7.30-7.38 (3H, m), 5.39 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378418B2
Source datasetuspto-grants-2008_05
ORD IDord-93c59fb79ae047b4aeab94af3e1abd4f
Source noteuspto-grants-2008_05