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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879916Generated: October 25, 2026

1,2-Diaminocyclohexane, trans- → 3-bromo-9-(dibenzo[b,d]furan-2-yl)-9H-carbazole

https://huagongshe.com/reaction/879916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-IododibenzofuranHCID 223327—
Reactant3-BromocarbazoleHCID 252446—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product3-bromo-9-(dibenzo[b,d]furan-2-yl)-9H-carbazoleHCID 5851100156.3%

Reaction Steps

A mixture of 8.9 g (36.2 mmole) 3-bromo-9H-carbazole, 10.6 g (36.2 mmole) of 2-iododibenzo[b,d]furan, 17.1 g (90 mmole) of copper(I) iodide, 19.1 g (90 mmole) of potassium phosphate, 10.3 g (90 mmole) of trans-1,2-cyclohexanediamine and 1,4-dioxane 700 ml were refluxed under nitrogen for about overnight. Then, the solution was filtered at 110° C. To receive the filtrate, And the 1,4-dioxane was removed under reduced pressure from the filtrate. The filtrate was extracted with 500 ml dichloromethane and 2000 ml water, the organic layer was dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-ethyl acetate) to give product 8.4 g (56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993130B2
Source datasetuspto-grants-2015_03
ORD IDord-8a9db235b26c47ad9e6e87a852b08f9e
Source noteuspto-grants-2015_03