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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811468Generated: November 1, 2026

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

https://huagongshe.com/reaction/1811468

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; Bortolatoi, A; Moro, S. Macchia, M. ChemMedChem, 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 numberUS08362277B2
Source datasetuspto-grants-2013_01
ORD IDord-7ccf7ae2b8fb4f96a56ad37be5474fe4
Source noteuspto-grants-2013_01