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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110662Generated: November 4, 2026

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

https://huagongshe.com/reaction/1110662

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 1N 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 numberUS04976773
Source datasetuspto-grants-1990_12
ORD IDord-3b259a2574ea40a788f6b3d4830be565
Source noteuspto-grants-1990_12