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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776206Generated: October 31, 2026

Potassium Hydroxide → 4,5-Difluoro-9-(oxiran-2-ylmethyl)-9H-carbazole

https://huagongshe.com/reaction/1776206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEpibromohydrinHCID 18430—
Reactant4,5-difluoro-9H-carbazoleHCID 68396795—
SolventDimethylformamideHCID 6228—
Product4,5-Difluoro-9-(oxiran-2-ylmethyl)-9H-carbazoleHCID 8989792893.5%

Reaction Steps

To a stirred solution of 4,5-difluoro-9H-carbazole (0.270 g, 1.3 mmol) in N,N-dimethylformamide (5 mL) at 0° C. was added 85% potassium hydroxide (0.105 g, 1.6 mmol) and the mixture was stirred for 1 hr. Epibromohydrin (0.220 mL, 2.7 mmol) was added and the mixture was slowly warmed to room temperature and stirred for 4 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 (0.315 g, 91%). 1H NMR (300 MHz, CDCl3) δ 7.45 (tt, 2H, J=8.1, 2.4 Hz), 7.25 (d, 2H, J=8.1 Hz), 6.99 (dt, 2H, J=9.9, 4.2 Hz), 4.68 (dd, 1H, J=15.9, 3.0 Hz), 4.38 (dd, 1H, J=15.9, 5.1 Hz), 3.37 (m, 1H), 2.85 (t, 1H, J=4.5 Hz), 2.57 (dd, 1H, J=4.5, 2.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265772B2
Source datasetuspto-grants-2016_02
ORD IDord-a7d3ef2969f749ef97d5ab408747eb49
Source noteuspto-grants-2016_02