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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776197Generated: October 25, 2026

Potassium Hydroxide → 2,7-Difluoro-9-(oxiran-2-ylmethyl)-9H-carbazole

https://huagongshe.com/reaction/1776197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEpibromohydrinHCID 18430—
Reactant2,7-difluoro-9H-carbazoleHCID 59326141—
SolventDimethylformamideHCID 6228—
Product2,7-Difluoro-9-(oxiran-2-ylmethyl)-9H-carbazoleHCID 8989756592%

Reaction Steps

To a stirred solution of 2,7-difluoro-9H-carbazole (0.400 g, 2.0 mmol) in N,N-dimethylformamide (5 mL) at 0° C. was added 85% potassium hydroxide (0.156 g, 2.4 mmol) and the mixture was stirred for 1 hr. Epibromohydrin (0.326 mL, 3.9 mmol) was added and the mixture was slowly warmed to room temperature and stirred for 16 hrs. The mixture was partitioned between water and ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried (anhydrous sodium sulfate), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (10-50% methylene chloride/hexanes) to afford the desired product as a white solid (0.47 g, 92%). 1H NMR (300 MHz, CDCl3) δ 7.93 (dd, 2H, J=8.4, 5.4 Hz), 7.14 (dd, 2H, J=9.9, 2.4 Hz), 6.99 (td, 2H, J=9.0, 2.4 Hz), 4.60 (dd, 1H, J=15.9, 2.7 Hz), 4.25 (dd, 1H, J=15.9, 5.1 Hz), 3.35 (m, 1H), 2.86 (t, 1H, J=4.5 Hz), 2.57 (dd, 1H, J=4.8, 2.7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265772B2
Source datasetuspto-grants-2016_02
ORD IDord-c6e9f90972004437b2f342719f8172ec
Source noteuspto-grants-2016_02