HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-(7-Bromo-9,9-dimethylfluoren-2-yl)dibenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dibenzo(b,d)furan-2-ylboronic Acid (contains varying amounts of Anhydride) | HCID 12032376 | — |
| Reactant | 2,7-Dibromo-9,9-dimethylfluorene | HCID 12123876 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Toluene water | HCID 22272177 | — |
| Product | 2-(7-Bromo-9,9-dimethylfluoren-2-yl)dibenzofuran | HCID 59866464 | 48% |
Reaction Steps
2,7-dibromo-9,9-dimethyl-9H-fluorene (5.0 g, 14.201 mmol), dibenzo[b,d]furan-2-ylboronic acid (1.50 g, 7.10 mmol), Pd(pph3)4 (820 mg, 0.71 mmol), K2CO3 (1.96 g, 14.201 mmol) were put in a 250 mL two-neck flask and dissolved in toluene/H2O. The solution was refluxed and stirred for 12 hours. After completion of the reaction, the solution was distilled under reduced pressure to remove the solvent. The resultant was columned with a solution of hexane and methylenechloride (8:1). The solution was distilled under reduced pressure and was re-crystallized in a solution of methylene chloride and petroleum ether such that the white solid compound was obtained, (1.50 g, yield: 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09281482B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-753e050ac221420586fa1138811bb106 |
| Source note | uspto-grants-2016_03 |