HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779132Generated: November 3, 2026
Potassium Hydroxide → 4,5-Diazafluoren-9-one
https://huagongshe.com/reaction/1779132
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,10-Phenanthroline hydrate | HCID 21226 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,5-Diazafluoren-9-one | HCID 342157 | 48% |
Reaction Steps
To a boiling solution of phenanthroline monohydrate (2.2 g, 11.1 mol) and KOH (2 g, 35.5 mol) in water (130 ml), a hot solution of KMnO4 (5 g, 31.5 mol) in water (80 ml) was added dropwise over ca. 1 h. The mixture was refluxed for another 2 h, and then filtered hot. The orange filtrate was cooled and extracted with chloroform, the combined organic extracts were dried over anhydrous Na2SO4. After solvent removal, the crude product was further purified by column chromatography on silica gel using acetone/petroleum ether (2:1) as the eluent, the product was isolated as a yellow solid (980 mg, 48%). 1HNMR (ACETONE-D6,400 MHz): δ=8.80(d, J=5.0 Hz, 2H), 8.06 (d, J=7.5 Hz, 2H), 7.50 (dd, J1=7.5 Hz, J2=5.0 Hz, 2H). HRMS calcd for 182.1782, found 182.0369.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09269908B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-8a1023c5a01e4cf9b238342957253482 |
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| Source note | uspto-grants-2016_02 |
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