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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
Reactant9-(3'-bromo-[1,1'-biphenyl]-3-yl)-9H-carbazoleHCID 58871153—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product9-(3'-iodo-[1,1'-biphenyl]-3-yl)-9H-carbazoleHCID 9038690896.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927749B2
Source datasetuspto-grants-2015_01
ORD IDord-e51b2b945f4a49018deab1531805da4c
Source noteuspto-grants-2015_01