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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619682Generated: October 29, 2026

Water → 2-Chloro-4'-fluorobiphenyl-4-ol

https://huagongshe.com/reaction/1619682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant4-Bromo-3-chlorophenolHCID 7018182—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-4'-fluorobiphenyl-4-olHCID 4631434294%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Fluorobenzeneboronic acid (405 mg, 2.89 mmol) and 4-bromo-3-chlorophenol (500 mg, 2.41 mmol) were dissolved in dioxane (15 mL) and water (3 mL) under nitrogen. The solution was degassed before tetrakis(triphenylphosphine) palladium (0) (278 mg, 0.24 mmol) was added followed by caesium carbonate (2.36 g, 7.23 mmol) and the reaction was stirred at 80° C. for 18 hours. The cooled reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was separated and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (20% ethyl acetate in heptane) to afford the title compound (503 mg, 94%) as a tan oil which solidified on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772293B2
Source datasetuspto-grants-2014_07
ORD IDord-30599fcb75374c4d8e09d49071735ca9
Source noteuspto-grants-2014_07