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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901697Generated: October 28, 2026

Water → 4-(6-Methoxy-naphthalen-2-yloxy)-1-nitrobenzene

https://huagongshe.com/reaction/901697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Methoxy-2-naphtholHCID 288634—
SolventDimethylformamideHCID 6228—
Product4-(6-Methoxy-naphthalen-2-yloxy)-1-nitrobenzeneHCID 66977464—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (20 mL) at rt, solid potassium carbonate (30 mmol) was added followed by addition of 6-methoxy-2-naphthol (10 mmol) to the reaction mixture and heating to 80° C. until the reaction was complete as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was poured into H2O (100 mL), extracted with EtOAc (2×50 mL), washed with H2O (2×50 mL) and brine (50 mL), and dried over sodium sulfate. The solvent was removed in vacuuo to afford the desired 4-(6-methoxy-naphthalen-2-yloxy)-1-nitrobenzene. The crude product was used for further transformation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361678B2
Source datasetuspto-grants-2008_04
ORD IDord-a00f0df7a8c246bc96998a3a6c09e836
Source noteuspto-grants-2008_04