HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → 6-[(4-Hydroxyphenyl)amino]-2-naphthalenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | 2,6-Dihydroxynaphthalene | HCID 93552 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-[(4-Hydroxyphenyl)amino]-2-naphthalenol | HCID 14499208 | 31.1% |
Reaction Steps
A mixture of 300 mg (2.75 mmol, Aldrich) of 4-aminophenol, 1.5 g (90%, 8.4 mmol, Aldrich) of 2,6-dihydroxynaphthalene and 1.0 g (9.6 mmol, Aldrich), of sodium bisulfite in 30 ml of H2O was refluxed for 18 hours. The reaction mixture was cooled, added to 30 ml of H2O and extracted with two 25 ml portions of ethyl acetate. The organic extracts were combined, dried (MgSO4), and concentrated in vacuo to give a solid. The crude solid was purified by flash chromatography (15×5.0 cm, 1:2 EtOAc/pet ether) followed by recrystallization (EtOAc/pet ether) to afford 215 mg (31%) of title compound as pale pink crystals, m.p. 195°-196°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04814454 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-923e4304ef314a089afc1df6a7a23b49 |
| Source note | uspto-grants-1989_03 |