HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424768Generated: November 1, 2026
Sodium Iodide → 9-(3'-iodo-[1,1'-biphenyl]-3-yl)-9H-carbazole
https://huagongshe.com/reaction/1424768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1-N,2-N-dimethylcyclohexane-1,2-diamine | HCID 551074 | — |
| Reactant | 9-(3'-bromo-[1,1'-biphenyl]-3-yl)-9H-carbazole | HCID 58871153 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 9-(3'-iodo-[1,1'-biphenyl]-3-yl)-9H-carbazole | HCID 90386908 | 96.1% |
Reaction Steps
9-(3′-bromo-[1,1′-biphenyl]-3-yl)-9H-carbazole (9.50 g, 23.85 mmol), sodium iodide (7.15 g, 47.7 mmol), copper(I) iodide (1.363 g, 7.16 mmol), and dioxane (239 ml) were added into a 500 mL 3-necked flask. N1,N2-dimethylcyclohexane-1,2-diamine (1.881 ml, 11.93 mmol) was added. The reaction mixture was heated and refluxed overnight. After completion of the reaction, the reaction mixture was cooled to room temperature. The reaction mixture was filtered through a pad of Celite® and washed several times with DCM. The solvent are evaporated in vacuum. The crude material was purified by column chromatography using hexane and DCM (75/25) and gradually increasing DCM to a ratio of hexane/DCM 50/50. The product was further purified by trituration from methanol. 9-(3′-iodo-[1,1′-biphenyl]-3-yl)-9H-carbazole (10.2 g, 22.91 mmol, 96% yield) was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927749B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-e51b2b945f4a49018deab1531805da4c |
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| Source note | uspto-grants-2015_01 |
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