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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384551Generated: November 1, 2026

2-Fluoro-5-methoxycarbonyloxy-4-methylnitrobenzene → 5-Amino-4-fluoro-2-methylphenyl Methoxyformate

https://huagongshe.com/reaction/1384551

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-methoxycarbonyloxy-4-methylnitrobenzeneHCID 14421619—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product5-Amino-4-fluoro-2-methylphenyl MethoxyformateHCID 2262504694.1%

Reaction Steps

A mixture of (4-fluoro-2-methyl-5-nitrophenyl) methyl carbonate (8 g, 35 mmol), (EP 0307777 A2), and platinum(IV)oxide (174 mg) in ethanol (100 ml) and ethyl acetate (70 ml) was stirred under hydrogen at 1.3 atmospheres pressure for 1.5 hours. The catalyst was removed by filtration through diatomaceous earth and the solvent removed by evaporation. The residue was purified by column chromatography eluting with petroleum ether/ethyl acetate (7/3) to give 2-fluoro-5-methoxycarbonyloxy-4-methylaniline (6.56 g, 94%) as an oil which crystallised. 1H NMR Spectrum (CDCl3): 2.09(s, 3H); 3.66(br s, 2H); 3.90(s, 3H); 6.54(d, 1H); 6.83(d, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-add2b1fbb4134c80a06fd654b18f453e
Source noteuspto-grants-2001_07