Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,10-Phenanthroline, 4,7-dimethyl- | HCID 72792 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21705494 | HCID 21705494 | 15% |
Reaction Steps
4,7-Dimethyl-1,10-phenanthroline (1 g, 4.8 mmol) was mixed well with 5.95 g (50 mmol) of potassium bromide and the mixture was placed in a 200 ml flask. The flask was cooled to 0° C., to which 20 ml of concentrated sulfuric acid was slowly added with stirring and, then, 10 ml of concentrated nitric acid was added in a similar manner. The reaction mixture was then heated at 80-85° C. for 2 hours. After being cooled to room temperature, the reaction mixture was poured into 400 ml of water. The aqueous solution was neutralized with sodium hydrogen carbonate, from which a product was extracted twice with 100 ml of methylene chloride. The extract was dried with anhydrous magnesium sulfate. The solvent was then removed by distillation to leave yellow solids. Recrystallization from methanol gave 172 mg of 4,7-dimethyl-1,10-phenanthroline-5,6-dione (2) with a yield of 15%. The structure of the product was confirmed by 1HNMR and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06288229B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-21115e9e1a034a26962779df81c0bb5d |
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| Source note | uspto-grants-2001_09 |
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