Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 178419810 | HCID 178419810 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 58979964 | HCID 58979964 | 17.8% |
Reaction Steps
Under nitrogen atmosphere, a mixture of 13 g (0.045 mol) 2,9-bis-(1H-tetrazol-5-yl)-[1,10]phenanthroline and 390 ml pyridine was added to a 250 ml three-necked flask. The mixture was then heated to 50° C., and 24.6 g (0.17 mol) benzoyl chloride was then added drop by drop. After the adding, the mixture solution was heated to reflux (110° C.) and stirred overnight. After completion of reaction, the reaction mixture was cooled to room temperature, filtered. Finally, solids were separated, washed by 100 ml methanol, filtered and purified by column chromatography to obtain white products 2,9-bis-(5-phenyl-[1,3,4]oxadiazol-2-yl)-[1,10]phenanthroline 4 g (0.008 mol, yield 17%). MS(m/z, FAB+), 468, 467, 307, 154, 105.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07282586B1 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-d2ee758ad1fb43bb903c3bdc81b85cd0 |
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| Source note | uspto-grants-2007_10 |
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