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Bamberger Rearrangement of <i>N</i>-Arylhydroxylamine to <i>p</i>-Aminophenol in a CO<sub>2</sub>–H<sub>2</sub>O System
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Citations
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References
2014
Year
Bamberger RearrangementBiosynthesisEngineeringCo2–h2o SystemBiochemistryAldo-keto ReductaseNatural SciencesBiocatalysisAldehyde DehydrogenaseOrganic ChemistryInorganic Strong AcidChemistryEnzymatic ModificationBiomolecular Engineering
The Bamberger rearrangement of N-aryllhydroxylamine was first realized in a CO2–H2O system. The yield of p-aminophenol was 80% when N-phenylhydroxylamine was heated at 100 °C for 1 h under 4 MPa CO2. The process fully avoids the need of inorganic strong acid and is environmentally benign.
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