Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099059Generated: October 30, 2026

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

https://huagongshe.com/reaction/2099059

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. There action 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 numberUS07569518B2
Source datasetuspto-grants-2009_08
ORD IDord-305e82e7868e451897c26a4c63a13165
Source noteuspto-grants-2009_08