HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthol → Naphthalene, 2-(2-nitrophenoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Naphthalene, 2-(2-nitrophenoxy)- | HCID 9280487 | 99.9% |
Reaction Steps
To a stirred solution of 2-hydroxynaphthalene (5 g, 34.7 mmol) in anhydrous tetrahydrofuran was added 2-fluoronitrobenzene (4.90 g, 34.7 mmol) at room temperature. The resultant mixture was heated at reflux overnight. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure, the residue was diluted with water, the resulting mixture was extracted twice with methylene chloride and the combined extracts were dried (MgSO4). The resultant organic layer was concentrated under reduced pressure to yield 9.2 g of the title compound of Step A as an oil. Rf 0.45 (silica gel, 4:1 hexane-ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962436 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-6006c8c328c44bcea5b53027a34b0c78 |
| Source note | uspto-grants-1999_10 |