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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057348Generated: October 25, 2026

5-Benzyloxy-2-fluoro-4-methylaniline → 5-Benzyloxy-2-fluoro-4-methylphenol

https://huagongshe.com/reaction/1057348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-2-fluoro-4-methylanilineHCID 21991068—
ReactantSodium NitriteHCID 23668193—
CatalystCopper oxideHCID 14829—
CatalystCopper(II) nitrate trihydrateHCID 9837674—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product5-Benzyloxy-2-fluoro-4-methylphenolHCID 2199104927%

Reaction Steps

The starting material 5-benzyloxy-2-fluoro-4-methylphenol, was obtained by adding a solution of sodium nitrite (1.68 g, 24 mmol) in water (3.5 ml), dropwise, to a solution of 5-benzyloxy-2-fluoro-4-methylaniline (4.7 g, 20 mmol) in acetic acid (82 ml) and 70% sulphuric acid (3.15 ml) cooled at 10° C. The mixture was stirred vigorously for 20 minutes, then a solution of copper(II)nitrate trihydrate (481 g, 2 mol) in water (790 ml) was added, followed by copper(II)oxide (3 g, 19 mmol). After stirring for 3 hours, the mixture was extracted with ethyl acetate. The organic layer was washed with water and then brine, dried (MgSO4) and the solvent evaporated. The resulting oil was purified by flash chromatography using petroleum ether/ether (85/15) as eluent to give 5-benzyloxy-2-fluoro-4-methylphenol as an orange oil (1.25 g, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514971B1
Source datasetuspto-grants-2003_02
ORD IDord-5f4d5c760cd54487b1a924c580c6727a
Source noteuspto-grants-2003_02