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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678395Generated: November 3, 2026

Phosphorus oxychloride → 3-Chloro-5-(3-chlorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine

https://huagongshe.com/reaction/1678395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5-(3-chlorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)-2H-pyridazin-3-oneHCID 57793935—
Product3-Chloro-5-(3-chlorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazineHCID 5779389297%

Reaction Conditions

Temperature110 °C

Reaction Steps

2.34 g of 5-(3-chlorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)-2H-pyridazin-3-one and 10 g of phosphorus oxychloride were mixed and stirred at 110° C. for 1 hour. The reaction mixture was allowed to cool down to room temperature and concentrated under reduced pressure. To the residue was added ethyl acetate and ice water, and was separated to two layer. The organic layer was washed sequentially with water and saturated brine, and dried over anhydrous sodium sulfate, then, concentrated under reduced pressure, to obtain 2.39 g of 3-chloro-5-(3-chlorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine (hereinafter, referred to as compound (xx) of the present invention).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008512B2
Source datasetuspto-grants-2011_08
ORD IDord-abb3c412c8854fecba38d964caab0e0c
Source noteuspto-grants-2011_08