HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925281Generated: October 27, 2026
2,7-Naphthalenediol → 7-(6,7-Dimethoxyquinolin-4-yloxy)naphthalen-2-ol
https://huagongshe.com/reaction/1925281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,7-Naphthalenediol | HCID 11397 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 7-(6,7-Dimethoxyquinolin-4-yloxy)naphthalen-2-ol | HCID 67520324 | — |
Reaction Steps
To a solution of naphthalene-2,7-diol (8.95 g, 55.88 mmol) in NMP (50 mL) in a sealed tube, was added 4-chloro-6,7-dimethoxyquinoline (5.0 g, 22.35 mmol). KOH (1.40 g, 24.58 mmol) was added, followed by copper powder (0.71 g, 11.18 mmol). The tube was sealed and the solution was stirred and heated to 150° C. for 24 h. The reaction was cooled to RT, diluted with water and extracted with EtOAc 3×. The combined organic layer was washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The crude material was purified by silica gel chromatography with 50% to 100% (95:5:0.5 EtOAc/MeOH/NH4OH) in Hexanes to give the titled compound. MS (ESI, pos. ion) m/z: 348.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08178557B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-dda78f7dcb354cee8c7885c2fc8871cf |
|---|
| Source note | uspto-grants-2012_05 |
|---|