HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923731Generated: October 29, 2026
Potassium Carbonate → 4-([1,1'-Biphenyl]-2 yl)-1H-indene
https://huagongshe.com/reaction/923731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Biphenyl-2-boronic acid | HCID 4589187 | — |
| Reactant | 4-Bromo-1H-indene | HCID 15637624 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-([1,1'-Biphenyl]-2 yl)-1H-indene | HCID 21918395 | 91% |
Reaction Steps
A mixture of compound 4 (40 g, 205 mmol, 1 equiv), (biphenyl-2-yl)boronic acid (81.2 g, 410 mmol, 2 equiv), powdered potassium carbonate (85 g, 615 mmol, 3 equiv), and bis(triphenylphosphine)palladium(II)dichloride (7.2 g, 10.3 mmol, 0.05 equiv), 1,4-dioxane (300 mL) and water (150 mL) was heated overnight at 80° C. The reaction was poured into 500 mL of water and extracted with ethyl acetate (3×400 mL). The combined organic layers were washed with saturated brine (300 mL), dried over sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified over silica gel (400 g) eluting with heptanes to give compound (8) (50 g, 91% yield) as a light-yellow oil that slowly turned to an off-white solid on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09279024B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-6ab990d6f9c0416a9a6948c54f5cff59 |
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| Source note | uspto-grants-2016_03 |
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