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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408215Generated: November 1, 2026

N-bromobutanimide → 3-Bromo-9-phenylcarbazole

https://huagongshe.com/reaction/2408215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant9-PhenylcarbazoleHCID 70851—
SolventAcetic AcidHCID 176—
Product3-Bromo-9-phenylcarbazoleHCID 1894262488%

Reaction Steps

Firstly, 24.3 g (100 mmol) of N-phenylcarbazole was dissolved in 600 ml of glacial acetic acid, and 17.8 g (100 mmol) of N-bromo succinic acid imide was slowly added thereto. The mixture was stirred for overnight at a room temperature. This glacial acetic acid solution was dropped in 1 L of ice water while stirring them. A precipitated white solid was washed three times with water. This white solid was dissolved in 150 ml of diethyl ether, and washed with a saturated sodium hydrogencarbonate solution and water. This organic layer was dried with magnesium sulfate, and filtered. The obtained filtrate was concentrated. The thus obtained residue was added with about 50 ml of methanol and uniformly dissolved therein by being irradiated with supersonic. This solution was left to precipitate a white solid. This solution was filtrated and the filtrate was dried to obtain 28.4 g (the yield: 88%) of 3-bromo-9-phenylcarbazole, which was a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815410B2
Source datasetuspto-grants-2014_08
ORD IDord-57fb2183993643beba54187d3890d59d
Source noteuspto-grants-2014_08