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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915192Generated: November 1, 2026

N-bromobutanimide → 3-Bromo-9-(naphthalen-1-yl)-9H-carbazole

https://huagongshe.com/reaction/1915192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant9-(1-Naphthyl)-9H-carbazoleHCID 626218—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-9-(naphthalen-1-yl)-9H-carbazoleHCID 5956114999%

Reaction Steps

In a 200-mL conical flask, 5.9 g (20 mmol) of 9-(1-naphthyl)-9H-carbazole was dissolved in a mixture solvent of 50 mL of toluene and 70 mL of ethyl acetate, and then 3.6 g (20 mmol) of N-bromosuccinimide (abbreviation: NBS) was added to this solution. The mixture was stirred at room temperature for 36 hours. After completion of the reaction, this mixture solution was washed with water, and magnesium sulfate was added thereto so that moisture was adsorbed. This suspension was filtrated, and the obtained filtrate was concentrated and collected. As a result, 7.4 g of white powder that was an objective substance was obtained in a yield of 99%. The synthesis scheme of Step 1 is shown in (F6-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614334B2
Source datasetuspto-grants-2013_12
ORD IDord-6fd3c7643a824cf99480c4f6a3ccd27f
Source noteuspto-grants-2013_12