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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678397Generated: October 30, 2026

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

https://huagongshe.com/reaction/1678397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)-2H-pyridazin-3-oneHCID 57793916—
Product3-Chloro-6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)pyridazineHCID 25271420—

Reaction Conditions

Temperature110 °C

Reaction Steps

19.77 g of 6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)-2H-pyridazin-3-one and 100 ml 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 chloroform 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 19.90 g of 3-chloro-6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)pyridazine (hereinafter, referred to as compound (xxii) of the present invention).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008512B2
Source datasetuspto-grants-2011_08
ORD IDord-4b57d23868d245fb980e1249ddbb086f
Source noteuspto-grants-2011_08