Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772391Generated: November 1, 2026

Carbazole → HCID 86710450, compound

https://huagongshe.com/reaction/1772391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Bromo-4-methylanisoleHCID 89143—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86710450HCID 8671045047%

Reaction Steps

2-Bromo-4-methylanisole (20.11 g, 100 mmol, 1 equiv) and carbazole (20.06 g, 120 mmol, 1.2 equiv) were dissolved in 1,4-dioxane (400 mL). Potassium phosphate tribasic (37.15 g, 175 mmol, 1.75 equiv), copper (I) iodide (0.95 g, 5 mmol, 0.05 equiv) and racemic trans-1,2-diaminocyclohexane (2.4 mL, 20 mmol, 0.2 equiv) were added and the reaction was refluxed for two days. The reaction was cooled to room temperature, then partitioned with ethyl acetate (200 mL) and water (300 mL). The aqueous layer was extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with saturated brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified over silica gel (150 g), eluting with 3% ethyl acetate in heptanes to give 9-(2-methoxy-5-methylphenyl)-9H-carbazole (13.5 g, 45% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249238B2
Source datasetuspto-grants-2016_02
ORD IDord-5200890bd9404d89a0d958d65f078382
Source noteuspto-grants-2016_02