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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816863Generated: November 4, 2026

Carbazole → 9-(4-Bromophenyl)carbazole

https://huagongshe.com/reaction/1816863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
ReactantO-XyleneHCID 7237—
Reactant1,4-DibromobenzeneHCID 7804—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventHexaneHCID 8058—
SolventToluene hexaneHCID 21889329—
Product9-(4-Bromophenyl)carbazoleHCID 2236139044.4%

Reaction Steps

4.30 g (25.7 mmole) of carbazole, 18.19 g (77.1 mmole) of p-dibromobenzene, 0.14 g of palladium acetate and 0.33 g of 1,1′-bisdiphenyl phosphinoferrocene, 3.46 g of (36.0 mmole) sodium t-butoxide and 43 ml o-xylene were put in a 200 ml three-necked flask, and refluxed under stirring for 15 hours and 30 minutes under argon flow. The reaction mixture was filtered using a filter packed with alumina to remove insoluble matter, the filter was washed with toluene and tetrahydrofuran successively. The filtrate and wash liquid were combined and condensed under reduced pressure. Hexane was added to the residue, followed by heating and stirring, then insoluble matter was removed by filtration, and the filtrate was vacuum dried. Hexane was added to the residue and deposited crystal was filtered off. The filtrate was condensed, and refined by silica gel column chromatography (eluent:hexane/toluene:3/1), recrystallized with hexane to give 3.68 g of a white crystal of 9-(4-bromophenyl)carbazole (yield: 44.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07597955B2
Source datasetuspto-grants-2009_10
ORD IDord-f3a67d2c03fe445e82d6b1bd6d479240
Source noteuspto-grants-2009_10