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
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 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| 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 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
| 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-fa8a76fc985649209197c262dabdddf6 |
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| Source note | uspto-grants-2008_04 |
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