Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromopyridine | HCID 14268 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 22675463 | HCID 22675463 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 9948724 | HCID 9948724 | 31.9% |
Reaction Steps
0.47 g of the compound obtained in Example 13a, 0.30 g of 4-bromo-pyridine, 0.80 g of KOH and 0.20 g of 18-crown-6-ether were added to 20 ml of dimethyl sulfoxide and heated to 150° C. for 8 hours. The reaction mixture was cooled, then added with water and extracted with ethyl acetate. The extract was dried over sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate) to obtain 0.19 g of the title compound (yield: 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787561B1 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-ef19cbf496f54f12a5fc449206a1343f |
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| Source note | uspto-grants-2004_09 |
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