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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900332Generated: October 30, 2026

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

https://huagongshe.com/reaction/900332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactant4-(4-Bromophenyl)dibenzo[b,d]furanHCID 59022098—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
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 2 N sodium carbonate (4.7 mL, 9.4 mmol) were added and then the reaction was heated to 100° C. (oil bath temp.) for 2-3 h 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 organic extracts were washed with 0.5 N hydrochloric acid, water and sat'd aq NaCl and then dried over anhyd MgSO4, filtered and concentrated in vacuo. Purification by flash column chromatography (10-20% ethyl acetate in heptane) afforded the title compound has a white solid (1.51 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358248B2
Source datasetuspto-grants-2008_04
ORD IDord-fa8a76fc985649209197c262dabdddf6
Source noteuspto-grants-2008_04