Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Carbazole | HCID 6854 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 1-bromo-3-iodo- | HCID 11561 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Dichloromethane cyclohexane | HCID 21916607 | — |
| Product | 9-(3-Bromophenyl)-9H-carbazole | HCID 58690888 | 82.4% |
Reaction Steps
Under nitrogen, carbazole (24.3 g, 1 eq.) is added to a flask together with 1-bromo-3-iodobenzene (98%; 75.3 g, 1.9 eq.), potassium carbonate (48.2 g, 2.5 eq.) and copper (1.77 g, 0.1 eq.). The reaction is heated to 150° C. and stirred at 150° C. for 48 h. The mixture is cooled to room temperature and diluted with 150 mL of methylene chloride. 100 mL of demineralized water are added to the mixture, which is stirred. Removal of the aqueous phase is followed by washing a further 2× with demineralized water (100 mL). The organic phase is dried over sodium sulfate and concentrated. The excess 1-bromo-3-iodobenzene is distilled off under reduced pressure. LC (SiO2; cyclohexane/methylene chloride 95:5) gives 37.1 g of product (82.4% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067919B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-2b5d18e84d704e6ab53ff9e2691e344b |
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| Source note | uspto-grants-2015_06 |
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