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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168618Generated: November 1, 2026

5-(4-benzyloxy-phenyl)-6-trifluoromethyl-2H-pyridazin-3-one → 4-(4-Benzyloxy-phenyl)-6-chloro-3-trifluoromethyl-pyridazine

https://huagongshe.com/reaction/2168618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-benzyloxy-phenyl)-6-trifluoromethyl-2H-pyridazin-3-oneHCID 67375576—
ReactantHCID 178479711HCID 178479711—
Product4-(4-Benzyloxy-phenyl)-6-chloro-3-trifluoromethyl-pyridazineHCID 86657777—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of the 5-(4-benzyloxy-phenyl)-6-trifluoromethyl-2H-pyridazin-3-one (0.491 mmol, 170 mg) and phosphorus(V) oxychloride may be heated at 90° C. for 2 h. The reaction mixture may be concentrated in vacuo, and ice may be added to the residue. The mixture may be neutralized with solid sodium bicarbonate and extracted with diethyl ether. Purification by column chromatography on silica gel gives 4-(4-benzyloxy-phenyl)-6-chloro-3-trifluoromethyl-pyridazine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045461B2
Source datasetuspto-grants-2015_06
ORD IDord-000ef35bc410414d92ac13dbeb18d7eb
Source noteuspto-grants-2015_06