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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782640Generated: October 30, 2026

Sodium Carbonate → 4'-Dibenzofuran-4-yl-biphenyl-4-carbaldehyde

https://huagongshe.com/reaction/1782640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactant4-(4-Bromophenyl)dibenzo[b,d]furanHCID 59022098—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product4'-Dibenzofuran-4-yl-biphenyl-4-carbaldehydeHCID 59696179—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 4-formylphenylboronic acid (0.9 g, 5.64 mmol) in ethanol (10 mL) was added to a stirred solution of the crude 4-(4-bromophenyl)-dibenzofuran (from the previous reaction) in toluene (40 mL). tetrakis-(Triphenylphosphine)palladium(0) (270 mg, 5 mol %) and 2N sodium carbonate (4.7 mL, 9.4 mmol) were added and the reaction was heated to 100° C. (oil bath temp.) for 2-3 hrs until complete (TLC control). The reaction mixture was cooled to room temperature and partitioned between water and ethyl acetate. The phases were separated, the aqueous phase being further extracted with ethyl acetate (2×20 mL). The combined extract was washed with 0.5 N hydrochloric acid, water and brine and then dried over anhydrous MgSO4, filtered and concentrated in vacuo. Purification of the product by flash column chromatography, using 10-20% ethyl acetate in hexane as eluent, afforded the title compound has a white solid (1.51 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498356B2
Source datasetuspto-grants-2009_03
ORD IDord-892c3d1426bd485caba0c509e21d7fd1
Source noteuspto-grants-2009_03