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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240812Generated: October 30, 2026

2-Fluoro-N-methyl-4-nitrobenzamide → 4-Amino-2-fluoro-N-methylbenzamide

https://huagongshe.com/reaction/240812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-N-methyl-4-nitrobenzamideHCID 53440632—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product4-Amino-2-fluoro-N-methylbenzamideHCID 4413952192%

Reaction Steps

A mixture of N-Methyl-2-fluoro-4-nitrobenzamide (Formula 38) (0.18 g, 0.91 mmol) and iron (0.31 g, 5.60 mmol) in ethyl acetate (5 mL) and acetic acid (5 mL) was refluxed for 1 h. The solid particles were filtered off. The filtrate was washed with water and extracted with ethyl acetate. The organic layer was dried over MgSO4, concentrated and the residue was purified with SiO2 column chromatography (dichloromethane:acetone, 95:5) to give N-Methyl-2-fluoro-4-aminobenzamide (Formula 39) (0.14 g, 92%) as an off-white solid. 1H NMR (acetone-d6) δ 2.86 (d, 3H, J=4.3), 5.50 (br s, 2H), 6.37 (dd, 1H, J=14.7 and 2.1), 6.50 (dd, 1H, J=8.6 and 2.1), 7.06 (br s, 1H), 7.68 (dd, 1H, J=8.8 and 8.8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648105B2
Source datasetuspto-grants-2014_02
ORD IDord-49ea7e2d1cdc4d59bef1b83ebe05a7f9
Source noteuspto-grants-2014_02