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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591005Generated: October 31, 2026

4-Methoxyphenol → p-(p-Nitrophenoxy)anisole

https://huagongshe.com/reaction/1591005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
ReactantPotassium HydroxideHCID 14797—
CatalystCopperHCID 23978—
Productp-(p-Nitrophenoxy)anisoleHCID 8063730.9%

Reaction Steps

4-Bromonitrobenzene (4.0 g), hydroquinone monomethyl ether (3.1 g), potassium hydroxide (1.5 g) and copper powder (0.1 g) were mixed and the reaction was carried out at 160° C. to 200° C. for 3 hours. After cooling to room temperature, the reaction mixture was extracted with benzene (100 ml), and the extract was washed with 1 N sodium hydroxide, water, and saturated aqueous sodium chloride After drying over magnesium sulfate, the solvent was evaporated under a reduced pressure and the residue obtained was purified by medium pressure column chromatography using silica gel, to obtain 4-(4-nitrophenoxy)phenol methyl ether (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05205855
Source datasetuspto-grants-1993_04
ORD IDord-3d4be8bb13cb48f28d3fca89e414599a
Source noteuspto-grants-1993_04