Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927102Generated: October 25, 2026

2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → 3,4-bis(Benzyloxy)-6-[(4-fluorophenyl)methyl]pyridazine

https://huagongshe.com/reaction/927102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant3,4-Bis(benzyloxy)-6-chloropyridazineHCID 12213474—
ReactantHCID 178505763HCID 178505763—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3,4-bis(Benzyloxy)-6-[(4-fluorophenyl)methyl]pyridazineHCID 7127042797%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 3,4-bis(benzyloxy)-6-chloropyridazine (Intermediate 1) (1 g, 3.06 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.117 g, 0.245 mmol) and palladium (II) acetate (0.027 g, 0.122 mmol) in tetrahydrofuran (6.12 ml) under nitrogen was added (4-fluorobenzyl)zinc(II) bromide (9.18 ml, 4.59 mmol) and the resulting red/brown mixture was heated at 65° C. for 24 hours. The reaction mixture was cooled, diluted with ethyl acetate and washed with saturated aqueous sodium bicarbonate solution, saturated ammonium chloride solution and brine. The organics were dried (MgSO4), filtered and solvent removed in vacuo to give a brown oil. The oil was purified by silica chromatography (eluting with 0-100% ethyl acetate in petrol) to yield the title compound (663 mg, 1.61 mmol, 97% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290456B2
Source datasetuspto-grants-2016_03
ORD IDord-79d2a819b452424ea811f23102e76484
Source noteuspto-grants-2016_03