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Organic reaction in water. Part 5.1 Novel synthesis of anilines by zinc metal-mediated chemoselective reduction of nitroarenes
70
Citations
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References
2001
Year
Zinc MetalChemical EngineeringOrganic SolventEngineeringNovel OrganocatalystsOrganic ReactionHalide SubstituentsOrganic ChemistryCatalysisNovel SynthesisChemistryHeterocycle ChemistrySynthetic ChemistryCatalytic Synthesis
Nitroarenes can be reduced in high yields to the corresponding anilines using zinc metal and NH4Cl in water without any organic solvent at 80 °C with a simple procedure at low cost. The procedure is powerful enough to reduce sterically hindered 2,6-dimethylnitrobenzene and is chemoselective for nitro groups; ester, amide and halide substituents on aromatic rings are unaffected.
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