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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057349Generated: November 3, 2026

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

https://huagongshe.com/reaction/1057349

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 numberUS06514971B1
Source datasetuspto-grants-2003_02
ORD IDord-bbb58d41f5fd4f15bdfb24a8ea8e3360
Source noteuspto-grants-2003_02