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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464873Generated: October 31, 2026

Carbazole → 9-(4-Bromophenyl)carbazole

https://huagongshe.com/reaction/1464873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
Reactant1,4-DibromobenzeneHCID 7804—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
CatalystCopper iodideHCID 83717—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Product9-(4-Bromophenyl)carbazoleHCID 2236139036.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

First, 56 g (240 mmol) of p-dibromobenzene, 31 g (180 mmol) of carbazole, 4.6 g (24 mmol) of copper iodide, 66 g (480 mmol) of potassium carbonate, and 2.1 g (8 mmol) of 18-crown-6-ether were put in a 300-mL three-neck flask, and nitrogen was substituted for air in the flask. Then, 8 mL of N,N′-dimethylpropyleneurea (abbreviation: DMPU) was added therein, and the mixture was stirred at 180° C. for 6 hours. After the reaction mixture was cooled to room temperature, a precipitate was removed by suction filtration. The filtrate washed with dilute hydrochloric acid, a saturated sodium hydrogen carbonate aqueous solution, and a saturated saline solution in this order and dried with magnesium sulfate. After being dried, the solution was filtered naturally and condensed, and an obtained oily substance was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) and recrystallized with chloroform and hexane; thus, 21 g of an objective light brown plate-shaped crystal of 9-(4-bromophenyl)carbazole was obtained (yield: 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999520B2
Source datasetuspto-grants-2015_04
ORD IDord-220cf5e9801340649b534d5f1e9df15e
Source noteuspto-grants-2015_04