Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059875Generated: October 25, 2026

Potassium Phosphate, Tribasic → 5-(4-(Trifluoromethyl)phenyl)pyridazin-3(2H)-one

https://huagongshe.com/reaction/2059875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Reactant5-Iodo-2,3-dihydropyridazin-3-oneHCID 16638330—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product5-(4-(Trifluoromethyl)phenyl)pyridazin-3(2H)-oneHCID 5795038739.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

Tricyclohexyl phosphine (16.6 μL, 0.02 mmol) was added to a mixture of 5-iodopyridazin-3(2H)-one (35 mg, 0.16 mmol), 4-(trifluoromethyl)phenylboronic acid (30 mg, 0.16 mmol), potassium phosphate tribasic (117 mg, 0.55 mmol), and palladium (II) acetate (3.5 mg, 0.02 mmol) in Toluene (0.8 mL) and Water (0.3 mL). The mixture was stirred at 100° C. for 22 hours. The reaction was diluted with CH2Cl2, filtered and concentrated. The crude was purified using HPLC (Phen Luna Axia C18 5μ 10:90:0.1 to 90:10:0.1 MeOH—H2O-TFA) to afford the desired product 5-(4-(trifluoromethyl)phenyl)pyridazin-3(2H)-one 18A (14.8 mg, 0.06 mmol, 39.1% yield) as a white solid. LC/MS 282 (M+H)+, tR 0.77 min (method 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278316B2
Source datasetuspto-grants-2012_10
ORD IDord-298cfe593174440d8b9f2ab3d35484b9
Source noteuspto-grants-2012_10