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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,7-NaphthalenediolHCID 11397—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product7-(6,7-Dimethoxyquinolin-4-yloxy)naphthalen-2-olHCID 67520324—

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-dda78f7dcb354cee8c7885c2fc8871cf
Source noteuspto-grants-2012_05