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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061318Generated: November 1, 2026

Toluene → 3-Bromo-9-phenylcarbazole

https://huagongshe.com/reaction/2061318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantN-bromobutanimideHCID 67184—
Reactant9-PhenylcarbazoleHCID 70851—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-9-phenylcarbazoleHCID 1894262499%

Reaction Steps

In a 1000 mL Erlenmeyer flask, 24 g (100 mmol) of 9-phenyl-9H-carbazole, 18 g (100 mmol) of N-bromosuccinimide, 450 mL of toluene, and 200 mL of ethylacetate were added, and the mixture was stirred at room temperature for 45 hours. After the reaction, the resulting mixture was washed with water, and the organic layer is dried with magnesium sulfate. The mixture was filtered, and the resulting filtrate was concentrated to give 32 g of the desired substance 3-bromo-9-phenyl-9H-carbazole in 99% yield. The synthetic scheme of 3-bromo-9-phenyl-9H-carbazole is shown in the scheme (C-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283055B2
Source datasetuspto-grants-2012_10
ORD IDord-579d7af1db214a7f8b43e31cc1234caa
Source noteuspto-grants-2012_10