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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485052Generated: October 30, 2026

Toluene → 4'-Fluorobiphenyl-4-carbaldehyde

https://huagongshe.com/reaction/1485052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant4-BromobenzaldehydeHCID 70741—
Reactant4-Fluorophenylboronic acidHCID 285645—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4'-Fluorobiphenyl-4-carbaldehydeHCID 139255096.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-bromobenzaldehyde (10.0 g), 4-fluorophenylboronic acid (11.3 g), tetrakis(triphenylphosphine)palladium(0) (3.12 g), sodium carbonate (28.6 g), toluene (150 mL), ethanol (70.0 mL) and water (70.0 mL) was stirred at 100° C. for 12 hours. After cooling the reaction mixture to room temperature, water was added and extraction with toluene was conducted twice. The combined organic layers were washed with saturated brine and dried over anhydrous magnesium sulfate. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography (n-hexane:ethyl acetate=90:10) and after adding n-hexane to the residue, the mixture was stirred. The precipitate was recovered by filtration and dried under reduced pressure to give the titled compound as a colorless solid (10.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-eba4a806730348c88dc12af58a7e8898
Source noteuspto-grants-2016_08