Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | HCID 69951340 | HCID 69951340 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21250019 | HCID 21250019 | — |
Reaction Steps
8-[2-Methoxycarbonyl-2-(2,2,2-trifluoroethylsulfonyl)-ethenylamino]quinoline (4 g) was added to diphenyl ether (100 ml) with stirring at 260° C., and stirring was continued for 2 hours. The mixture was allowed to cool to ambient temperature and hexane (100 ml) was added. The mixture was filtered, and the residue purified by flash chromatography on silica using increasingly polar mixtures of methanol and chloroform as eluant. The product so obtained was recrystallised from acetic acid to give 3-(2,2,2-trifluoroethyl-sulfonyl)-4-oxo-3,4-dihydro-1,10-phenanthroline, mp 272-274° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06200974B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-72a7e2577b0c4eb5bac6ad22411ea7bf |
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| Source note | uspto-grants-2001_03 |
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