HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486376Generated: October 25, 2026
Potassium Carbonate → 9-(4-(8-bromodibenzo[b,d]furan-2-yl)phenyl)-9H-carbazole
https://huagongshe.com/reaction/1486376
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2,8-Dibromodibenzofuran | HCID 82290 | — |
| Reactant | 9-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole | HCID 11850073 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Water | HCID 962 | — |
| Product | 9-(4-(8-bromodibenzo[b,d]furan-2-yl)phenyl)-9H-carbazole | HCID 117607253 | 70.5% |
Reaction Steps
A mixture of Compound 11 (2.00 g, 4.56 mmol), 2,8-dibromodibenzo[b,d]furan (2.60 g, 7.98 mmol), tetrakis(triphenylphosphine) palladium(0) (0.26 g, 0.23 mmol), potassium carbonate (1.892 g, 13.70 mmol), 1,4-dioxane (60.00 mL), and water (12.00 mL) was degassed with bubbling argon for 1 hour. The reaction mixture was then heated to 80° C. and was stirred overnight (16.5 hours), maintaining an argon atmosphere. Consumption of the starting material was confirmed by thin-layer chromatography and the reaction was cooled to room temperature. The product was extracted with dichloromethane, dried, and purified by silica gel column chromatography with dichloromethane in hexanes as the eluent. The product fractions were then dried and the product was collected to yield Compound 13 (1.57 g, 70%). Confirmed by LCMS (APCI): calculated for C30H18BrNO (M+H): 488. Found: 488.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09425408B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4a6647a0dcde4912a868e38fb57a2e91 |
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| Source note | uspto-grants-2016_08 |
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