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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037509Generated: November 2, 2026

Carbazole → 1,3-Bis(N-carbazolyl)benzene

https://huagongshe.com/reaction/1037509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 1,3-diiodo-HCID 12270—
Reactant18-Crown-6HCID 28557—
Solvent1,2-DichlorobenzeneHCID 7239—
Product1,3-Bis(N-carbazolyl)benzeneHCID 22020377—

Reaction Steps

To a solution of 1,3-diiodobenzene (50.0 g, 0.152 mol), carbazole (55.0 g, 0.329 mol), Cu (40.0 g, 0.630 mol) and 18-crown-6 (0.5 g) in 1,2-dichlorobenzene (200.0 ml) was added potassium carbonate (150.0 g, 1.085 mol) under nitrogen and stirring. The reaction was carried out at 190° C. for 12 hours. After cooling, the reaction mixture was filtrated. The solid residues were carefully washed with THF. Then, THF and 1,2-dichlorobenzene were evaporated from the combined filtration solution. The crude product was purified by recrystallization from acetone/methanol to give 47.0 g (75.7%) in yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546505B2
Source datasetuspto-grants-2013_10
ORD IDord-d4c66e6e4da54063a83a6b554a01f228
Source noteuspto-grants-2013_10