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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393593Generated: October 26, 2026

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

https://huagongshe.com/reaction/393593

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 Conditions

Temperature10 °C

Reaction Steps

A solution of sodium nitrite (1.68 g, 24 mmol) in water (3.5 ml) was added to a solution of 5-benzyloxy-2-fluoro-4-methylaniline (4.7 g, 20 mmol) in acetic acid (25 ml) and 70% sulphuric acid (25 ml) at 10° C. The mixture was stirred at 10° C. for 20 minutes and a solution of copper(II)nitrate trihydrate (481 g, 2 mol) in water (790 ml) followed by copper(II)oxide (3 g, 19 mmol) was added. The mixture was stirred for 3 hours then extracted with ethyl acetate. The organic layer was washed with water, brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with petroleum ether/ether (85/15) to give 5-benzyloxy-2-fluoro-4-methylphenol (1.25 g, 27%) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809097B1
Source datasetuspto-grants-2004_10
ORD IDord-7113a17c42294fafb4f7216afb6af101
Source noteuspto-grants-2004_10