HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorophenol → 4-(4-Fluorophenoxy)-1,5-naphthyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | 4-Chloro-1,5-naphthyridine | HCID 596262 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-(4-Fluorophenoxy)-1,5-naphthyridine | HCID 19737869 | 47.1% |
Reaction Steps
A mixture comprising 150 mg (0.911 mmole) of 4-chloro-1,5-naphthyridine and 1.00 g of 4-fluorophenol was heated at 160° C. After one hour, the mixture was cooled and dissolved in ethyl acetate and 2N sodium hydroxide. The organic layer was washed twice with base to remove excess 4-fluorophenol. The organic layer was then dried with magnesium sulfate and concentrated, producing an oil that slowly crystallized. This product was recrystallized in heptane, giving 103 mg of the title product. MP 122°-124° C. Yield 47%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05240916 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-4a9ff2caa72f492a8f9c458e6cc984e4 |
| Source note | uspto-grants-1993_08 |