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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444664Generated: October 26, 2026

Toluene → 3-Bromo-9-phenylcarbazole

https://huagongshe.com/reaction/444664

Reaction equation

Participants

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

Reaction Steps

Into a 1000 mL three-neck flask were put 24 g (100 mmol) of 9-phenylcarbazole, 18 g (100 mmol) of N-bromosuccinimide, 450 mL of toluene, and 200 mL of ethyl acetate, and the mixture was stirred for 45 hours at room temperature. This suspending solution was washed with water, and magnesium sulfate was added therein, so that moisture was removed. Then, the suspending solution was filtered to provide a filtrate was obtained. The obtained filtrate was concentrated and dried, whereby 32 g of a caramel-like solid of 3-bromo-9-phenyl-9H-carbazole, which was the object of the synthesis, was obtained in a yield of 99% (synthesis scheme (a-6)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08475935B2
Source datasetuspto-grants-2013_07
ORD IDord-2684c3753105439598e448632ab069ea
Source noteuspto-grants-2013_07