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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619621Generated: October 31, 2026

4-Iodophenol → 4-(3-Trifluoromethylphenyl)phenol

https://huagongshe.com/reaction/1619621

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodophenolHCID 10894—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product4-(3-Trifluoromethylphenyl)phenolHCID 2009959730.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

An aqueous solution of sodium hydrogen carbonate (6.9 g in 18 mL water, 82 mmol) was added to a stirred solution of 3-trifluoromethylbenzeneboronic acid (7.77 g, 41 mmol) and 4-iodophenol (6.0 g, 30 mmol) in 1,4-dioxane (90 mL). The reaction mixture was degassed, then tetrakis(triphenylphosphine) palladium (0) (1.58 g, 1.36 mmol) was added and the reaction mixture heated at 100° C. for 18 hours. The mixture was diluted with a 2M aqueous solution of HCl and extracted with ethyl acetate (50 mL). The organic layer was separated, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (5%-40% ethyl acetate in heptane gradient elution) to afford the title compound (2.17 g, 30%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772293B2
Source datasetuspto-grants-2014_07
ORD IDord-0f79d83225b7446186e4194d4f1a7b87
Source noteuspto-grants-2014_07