Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220642Generated: October 31, 2026

Cesium fluoride → HCID 23134310, compound

https://huagongshe.com/reaction/2220642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant4-Carboxyphenylboronic AcidHCID 312183—
ReactantHCID 23134197HCID 23134197—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23134310HCID 23134310100%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-(4-bromo-2,3-dimethylphenoxy)ethanol (0.531 g), 4-carboxyphenylboronic acid (0.360 g), tetrakis-(triphenylphosphine)palladium(0) (0.125 g), cesium fluoride (1.645 g), water (2 mL), ethanol (2 mL) and 1,4-dioxane (8 mL) was stirred at 80° C. for 3 hrs. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to afford 4′-(2-hydroxyethoxy)-2′,3′-dimethylbiphenyl-4-carboxylic acid (0.62 g) as a crude product. A mixture of the crude 4′-(2-hydroxyethoxy)-2′,3′-dimethylbiphenyl-4-carboxylic acid, benzyl bromide (0.445 g), and potassium carbonate (0.450 g) in N,N-dimethylformamide (20 mL) was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/2) to afford the title compound (0.033 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417169B2
Source datasetuspto-grants-2008_08
ORD IDord-aabd8a0686524db5afa16e409514ea15
Source noteuspto-grants-2008_08