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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750851Generated: November 1, 2026

Methyl 4-fluoro-5-methyl-2-nitrobenzoate → Methyl 2-amino-4-fluoro-5-methylbenzoate

https://huagongshe.com/reaction/1750851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-fluoro-5-methyl-2-nitrobenzoateHCID 58115689—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 2-amino-4-fluoro-5-methylbenzoateHCID 5811558251.4%

Reaction Steps

The solution of crude methyl 4-fluoro-5-methyl-2-nitrobenzoate (5 g) in MeOH (50 mL) was hydrogenated using 10% Pd/C (0.5 g) as catalyst at atmospheric pressure overnight. The catalyst was removed by filtration, and the solvent was evaporated at reduced pressure. The residue was purified by column chromatography on silica gel eluted with PE-EA (8:1) to give methyl 2-amino-4-fluoro-5-methylbenzoate (2.21 g, yield 50% over three steps) as a white solid. 1H NMR (500 MHz, CDCl3) δ 7.715 (d, J=9.0 Hz, 1H), 6.339 (d, J=11.5 Hz, 1H), 3.873 (s, 3H), 2.154 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156860B2
Source datasetuspto-grants-2015_10
ORD IDord-b1168a31c78a409bb3f249486351fcda
Source noteuspto-grants-2015_10