Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 21462566 | HCID 21462566 | — |
| Reactant | HCID 21462587 | HCID 21462587 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 161229-62-5 | HCID 9929430 | — |
Reaction Steps
2-(2,2-bis(Difluoromethyl)-6-nitro-3,4-dihydro-2H-1,4-benzoxazine-4-yl)pyridine. The product of step c. (0.81 g) potassium carbonate (1.6 g), copper bronze (0.37 g), 2-bromopyridine (0.83 mL), 18-crown-6 (0.079 g), and 1,2-dichlorobenzene (8 mL) were stirred and heated at 170° C. for six hours. The reaction mixture was cooled, diluted with dichloromethane and chromatographed, eluting with dichloromethane, to give the pyridine as a light amber syrup (0.77 g); NMR: 4.34 (s,2), 6.55 (t,2), 7.07 (m,1), 7.37 (m,2), 7.82 (m,2), 8.23 (s,1), 8.39 (d,1); MS: m/z=358(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05486515 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-35e77f1eaae64093b9a0d391caf44c30 |
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| Source note | uspto-grants-1996_01 |
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