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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619627Generated: October 25, 2026

Potassium Carbonate → 3-Pyridazin-4-yl-4'-(trifluoromethyl)biphenyl-4-ol

https://huagongshe.com/reaction/1619627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Reactant4-Chloro-2-pyridazin-4-ylphenolHCID 136200875—
CatalystBis(tri-tert-butylphosphine)palladium(0)HCID 2734558—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
SolventSodium chloride; waterHCID 57417360—
Product3-Pyridazin-4-yl-4'-(trifluoromethyl)biphenyl-4-olHCID 13620088841%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-chloro-2-pyridazin-4-ylphenol (Preparation 7, 1.5 g, 7.26 mmol) and 4-trifluoromethylbenzene boronic acid (3.45 g, 18.1 mmol) in 1,4-dioxane (20 mL) was added a solution of potassium carbonate (2.0 g, 14.5 mmol) in water (4 mL). The reaction mixture was degassed, then bis(tri-t-butylphosphine) palladium (0) (371 mg, 0.726 mmol) added and the reaction mixture heated to 100° C. for 18 hours. The mixture was diluted with a 2M aqueous solution of hydrogen chloride and brine, then extracted with ethyl acetate. The organic layer was separated and dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (0%-100% ethyl acetate in dichloromethane gradient elution) to afford the title compound as a solid (940 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772293B2
Source datasetuspto-grants-2014_07
ORD IDord-02938912a8d8433d9cf3f6613adbdd96
Source noteuspto-grants-2014_07