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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7496Generated: October 26, 2026

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

https://huagongshe.com/reaction/7496

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-2-fluoro-4-methylnitrobenzeneHCID 21991057—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-Benzyloxy-2-fluoro-4-methylanilineHCID 2199106887.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

The starting material, 5-benzyloxy-2-fluoro-4-methylaniline, was obtained by adding iron powder (2.88 g, 51 mmol), in portions, to a solution of 5-benzyloxy-2-fluoro-4-methylnitrobenzene (4.8 g, 18 mmol) in acetic acid (33 ml) and water (5.7 ml), at ambient temperature. The mixture was heated and after stirring at 100° C. for 10 minutes, it was cooled and partitioned between ethyl acetate and water. The organic layer was washed with water, aqueous saturated sodium carbonate solution and then brine, dried (MgSO4) and the solvent evaporated. The residue was purified by flash chromatography using petroleum ether/ethyl acetate (8/2) as eluent to give 5-benzyloxy-2-fluoro-4-methylaniline (3.65 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087602B2
Source datasetuspto-grants-2006_08
ORD IDord-c8db631387344b1d934a549994ef9606
Source noteuspto-grants-2006_08