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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | 4,5-difluoro-9H-carbazole | HCID 68396795 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,5-Difluoro-9-(oxiran-2-ylmethyl)-9H-carbazole | HCID 89897928 | 93.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09265772B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-a7d3ef2969f749ef97d5ab408747eb49 |
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| Source note | uspto-grants-2016_02 |
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