HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbazole → 2-Bromo-8-carbazolyldibenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbazole | HCID 6854 | — |
| Reactant | 1,2-Diaminocyclohexane, trans- | HCID 43806 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2,8-Dibromodibenzofuran | HCID 82290 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Bromo-8-carbazolyldibenzofuran | HCID 66735887 | 32.3% |
Reaction Steps
A three-necked flask was charged with 2,8-dibromodibenzofuran (39.12 g, 120 mmol), carbazole (20.07 g, 120 mmol), K3PO4 (50.94 g, 240 mmol), copper iodide (11.43 g, 60 mmol), 1,2-trans-diaminocyclohexane (20.55 g, 180 mmol), and 1,4-dioxane (120 ml), and the mixture was refluxed for 9 h. After the reaction, the reaction product solution was cooled to room temperature and extracted with CH2Cl2 using a separatory funnel. The extract was dried over anhydrous magnesium sulfate, filtrated and concentrated. The obtained solid product was purified by a column chromatography (hexane:toluene=8:2). The above operations were all performed in an argon atmosphere (16.0 g, 32% yield),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114530B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-3c7cd744b3c14bd9af27638f340fbbf7 |
| Source note | uspto-grants-2012_02 |