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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332077Generated: November 1, 2026

Potassium Hydroxide → 3,6-dibromo-9-((oxiran-2-yl)methyl)-9H-carbazole

https://huagongshe.com/reaction/332077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEpibromohydrinHCID 18430—
Reactant3,6-DibromocarbazoleHCID 274874—
SolventDimethylformamideHCID 6228—
Product3,6-dibromo-9-((oxiran-2-yl)methyl)-9H-carbazoleHCID 277547366.3%

Reaction Steps

Following a literature procedure (Asso, V.; Ghilardi, E.; Bertini, S.; Digiacomo, M.; Granchi, C.; Minutolo, F.; Rapposelli, S.; Bortolato, A.; Moro, S. Macchia, M. Chem Med Chem, 2008, 3, 1530-1534) powdered KOH (0.103 g, 1.85 mmol) was added to a solution of 3,6-dibromocarbazole (0.500 g, 1.54 mmol) in DMF (1.5 mL) at ambient temperature and stirred for 30 min until dissolved. Epibromohydrin (0.32 mL, 3.8 mmol) was added via syringe and the reaction was stirred at room temperature overnight. Upon completion, the solution was partitioned between EtOAc and H2O. The aqueous layer was washed 3× with EtOAc, and the combined organics were washed with saturated aqueous NaCl, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was recrystallized from EtOAc/Hexane to afford the desired product (389 mg, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877797B2
Source datasetuspto-grants-2014_11
ORD IDord-3fc1adc4c90e4c4c959017eda7ff1c27
Source noteuspto-grants-2014_11