HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900342Generated: October 29, 2026
Sodium Carbonate → 4'-Dibenzofuran-4-yl-biphenyl-4-carbaldehyde
https://huagongshe.com/reaction/900342
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Reactant | 4-(4-Bromophenyl)dibenzo[b,d]furan | HCID 59022098 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4'-Dibenzofuran-4-yl-biphenyl-4-carbaldehyde | HCID 59696179 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358248B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-e5503b2a6dfc4e27be473a1afc5250bd |
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| Source note | uspto-grants-2008_04 |
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