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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547844Generated: October 30, 2026

4-Iodophenol → 4',5'-Difluoro-2'-methoxy-biphenyl-4-ol

https://huagongshe.com/reaction/547844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodophenolHCID 10894—
ReactantPotassium CarbonateHCID 11430—
Reactant(4,5-Difluoro-2-methoxyphenyl)boronic acidHCID 16217679—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4',5'-Difluoro-2'-methoxy-biphenyl-4-olHCID 5825999389.3%

Reaction Conditions

Temperature82.5 °C

Reaction Steps

4,5-Difluoro-2-methoxyphenyl-boronic acid (8.8 g, 46.82 mmol) and 4-iodophenol (6.86 g, 31.21 mmol) were suspended in 165 ml of DMF. H2O (40 mL) was added and the mixture was degassed with argon. Finely ground potassium carbonate (13 g, 93.63 mmol) and tetrakis(triphenylphosphine) palladium(0) (1.5 g, 1.29 mmol) were added. The reaction was stirred at 80-85° C. for 1 hr under argon and cooled. The mixture was diluted with ethyl acetate and water. The organic layer was washed with brine, dried and solvents were evaporated. The crude product was purified by flash chromatography, eluting with 0-8% ethyl acetate in hexanes to yield 4′,5′-difluoro-2′-methoxy-biphenyl-4-ol (6.58 g, 89.3%). LR-MS (ES) calculated for C13H10F2O, 236.22; found m/z 235 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939569B1
Source datasetuspto-grants-2011_05
ORD IDord-ca1b55e1aeb742eca7e378533e6547e1
Source noteuspto-grants-2011_05