HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180680Generated: October 31, 2026
4-Phenylbenzoyl chloride → HCID 58979977, compound
https://huagongshe.com/reaction/1180680
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Phenylbenzoyl chloride | HCID 84151 | — |
| Reactant | HCID 178419810 | HCID 178419810 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 58979977 | HCID 58979977 | 80% |
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 46 g (0.21 mol) 4-phenylbenzoyl 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, as shown in scheme 2, 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-biphenyl-4-yl-[1,3,4]oxadiazol-2-yl)-[1,10]phenanthroline 11 g (0.018 mol, yield 40%). MS(m/z, FAB+), 620, 291, 248, 233, 208, 156, 130, 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-839940281542488f9445d8b8c356b2a4 |
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| Source note | uspto-grants-2007_10 |
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