HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113192Generated: October 29, 2026
Potassium Carbonate → HCID 59655978, compound
https://huagongshe.com/reaction/2113192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Silane, (4-bromophenyl)trimethyl- | HCID 138897 | — |
| Reactant | Dibenzofuran-4-boronic acid | HCID 2734328 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59655978 | HCID 59655978 | 96.8% |
Reaction Steps
A solution of dibenzofuran-4-yl-boronic acid (20.0 g, 94.3 mmol), (4-bromo-phenyl)-trimethyl-silane (21.62 g, 94.3 mmol), K2CO3 (39.1 g, 3 equiv., 283 mmol) in toluene (100 mL), ethanol (60 mL) and water (30 mL) was purgged with nitrogen for 5 min (bubbled into solution) and treated with Pd(PPh3)4 (3.59 g, 2.9 mmol). After heating to 80° C. for 4 h, the solution was cooled to room temperature, poured into water (300 mL) and extracted with ethyl acetate (300 mL). The organic phase was washed with sat'd aq NaCl, dried over anhydrous MgSO4, filtered and concentrated in vacuo. Purification by flash column chromatography (5-20% ethyl acetate in heptane) afforded (4-dibenzofuran-4-yl-phenyl)-trimethyl-silane as a colorless oil (28.9 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524878B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-2cd49644adb04c0c93692aa07eaf5d9f |
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| Source note | uspto-grants-2009_04 |
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