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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619664Generated: October 30, 2026

Water → 4′-Chloro-3′-(trifluoromethyl)[1,1′-biphenyl]-4-ol

https://huagongshe.com/reaction/1619664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant4-IodophenolHCID 10894—
Reactant4-Chloro-3-(trifluoromethyl)benzeneboronic acidHCID 2782671—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product4′-Chloro-3′-(trifluoromethyl)[1,1′-biphenyl]-4-olHCID 2300508827.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Chloro-3-(trifluoromethyl)phenylboronic acid (448 mg, 2 mmol) and 4-iodophenol (440 mg, 2 mmol) were dissolved in dioxane (10 mL). Caesium carbonate (1.95 g, 6 mmol), water (2 mL) and tetrakis(triphenylphosphine)palladium (0) (231 mg, 0.2 mmol) were added and the reaction stirred at 80° C. for 1 hour. The reaction was quenched with 2M HCl (5 mL) and partitioned between ethyl acetate (50 mL) and water (50 mL). The ethyl acetate was separated, dried over MgSO4 and evaporated. The crude product was chromatographed on silica eluting with a gradient of heptane:ethyl acetate 100:0 to 80:20 to give the title compound (150 mg, 0.55 mmol, 27%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772293B2
Source datasetuspto-grants-2014_07
ORD IDord-3307399c6f5a4f26bf5a0fc075e89d7a
Source noteuspto-grants-2014_07