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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947850Generated: November 4, 2026

5-Fluoro-N-methyl-2-nitrobenzamide → 2-Amino-5-fluoro-N-methylbenzamide

https://huagongshe.com/reaction/1947850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-N-methyl-2-nitrobenzamideHCID 44203077—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-Amino-5-fluoro-N-methylbenzamideHCID 43132558100%

Reaction Steps

A solution of 5-fluoro-N-methyl-2-nitrobenzamide (Compound 102B) in EtOH (10.0 mL) was charged with Palladium 10% wt on activated carbon (0.316 g, 0.297 mmol). The reaction mixture was evacuated and purged with hydrogen gas (3 times). The reaction mixture was allowed to stir under hydrogen at rt for 16 h. The reaction mixture was filtered through a pad of celite. The filtrate was concentrated under reduced pressure to yield a light yellow semi-solid. The material was purified by silica gel chromatography using DCM/MeOH (100:0→95:5) as eluent. The fractions containing product were combined and concentrated under reduced pressure to yield a white solid, 0.500 g (100% yield). 1H NMR (CDCl3, 400 MHz): δ=2.98 (d, J=4.80 Hz, 3H), 5.30 (d, J=5.31 Hz, 1H), 6.64 (dd, J=8.84, 4.80 Hz, 1H), 6.96 (ddd, J=8.91, 7.89, 2.91 Hz, 1H), 7.02 (dd, J=9.22, 2.91 Hz, 1H). MS (ES+): m/z 169.08 [MH+] (TOF, polar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399433B2
Source datasetuspto-grants-2013_03
ORD IDord-2551509369d84dd0bdae3c365b124c90
Source noteuspto-grants-2013_03