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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619697Generated: November 1, 2026

Water → 2-Chloro-2'-fluoro-5-methoxybiphenyl

https://huagongshe.com/reaction/1619697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant2-Fluorophenylboronic acidHCID 2734354—
Reactant2-Bromo-1-chloro-4-methoxybenzeneHCID 24212081—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-2'-fluoro-5-methoxybiphenylHCID 5804229888.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

Tetrakistriphenylphosphinepalladium (0) (229 mg, 0.20 mmol) was added to a degassed mixture of 2-fluorophenylboronic acid (556 mg, 3.97 mmol), 2-bromo-1-chloro-4-methoxybenzene (0.49 mL, 3.57 mmol), caesium carbonate (3.87 g, 11.9 mmol), water (5.0 mL) and dioxane (26.0 mL). The reaction was heated at 80° C. for 18 hours, cooled to room temperature and then partitioned between ethyl acetate (30.0 mL) and sat. aq. ammonium chloride (10.0 mL). The aqueous phase was separated and extracted with ethyl acetate (2×10 mL). The combined organic phases were washed with brine (5.0 mL), dried over MgSO4, filtered and evaporated to give a pale yellow oil. Column chromatography purification on silica, eluting with heptanes gave the title compound (749 mg, 88%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772293B2
Source datasetuspto-grants-2014_07
ORD IDord-d8d4b2361e5147d793efdc9c007bc1eb
Source noteuspto-grants-2014_07