HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-2-[4-(trifluoromethyl)phenyl]pyridine → 7-[2-(4-Trifluoromethyl-phenyl)-pyridin-4-yloxy]-quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-2-[4-(trifluoromethyl)phenyl]pyridine | HCID 21865292 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 7-Hydroxyquinoline | HCID 135426866 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 7-[2-(4-Trifluoromethyl-phenyl)-pyridin-4-yloxy]-quinoline | HCID 59735754 | — |
Reaction Steps
This material was prepared following the methods described in Example 8 (b) using 4-chloro-2-(4-trifluoromethyl-phenyl)-pyridine (Example 8 (a), 43 mg, 0.16 mmol), 7-hydroxyquinoline (46 mg, 0.32 mmol) and potassium t-butoxide (38 mg, 0.34 mmol) in N-methylpyrrolidone (0.6 mL). The compound was purified by flash chromatography using 1:4 of EtOAc/hexanes, to provide the title compound as a white solid. MS (ESI, pos. ion) m/z: 367 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07390907B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-9fcd5c9b2c87439285e838f1304eed0c |
| Source note | uspto-grants-2008_06 |