Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Quinoline, 7,8-Difluoro- | HCID 3025799 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 68285982 | HCID 68285982 | 70% |
Reaction Steps
In a 3 L eggplant-shaped flask containing a stir bar, 7,8-difluoroquinoline (185.5 g, 1.12 mol), N-iodosuccinimide (505.4 g, 2.25 mol), and acetic acid (927 mL) were introduced and the mixture was stirred for 30 hours at 90° C. After cooling, the precipitated crystals was filtered and dried. On the other hand, the filtrate was concentrated under reduced pressure, the residual acetic acid was neutralized with sodium hydrogen carbonate, and the resultant was subjected to extraction with ethyl acetate. In addition, after the filtrate was dried with magnesium sulfate, filtered and concentrated, the thus obtained crude product was purified by silica gel column chromatography (normal hexane:ethyl acetate) to obtain 227.2 g (70%) of 7,8-difluoro-3-iodoquinoline was obtained as a hazel solid combined with the previously obtained crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772200B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-bcad5431f40e4f55b2f07caf664d8a37 |
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| Source note | uspto-grants-2014_07 |
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