We studied the influence of temperature, solvent, pressure, catalysts type on the selectivity of nitrobenzenehydrogenation to cyclohexanone oxime (COX) in the presence of NH2OH. The best reaction conditions are:pressure 0.8 MPa, temperature 333 K, solvent ethers, and catalyst Pd/C5%. Other hydrogenation metal catalystsdid not give comparable results. The amount of Pd/C influences the yield in COX, which rises above to 90 % atthe highest load. The reaction profile shows that aniline is the reaction intermediate. Indeed, aniline as a sub-strate gives COX, though in lower yield than that achieved employing nitrobenzene. The NH2OH parallel hy-drogenation to NH4Cl, influences positively the selectivity to COX. It has been observed that COX, cyclohex-anone and N-cyclohexylideneaniline are in equilibrium in the reaction solution and all likely derive fromnucleophilic substitutions to a common imine intermediate formed on the Pd surface, whose high activity doesnot need any further metal catalyst

Pd/C Catalyzed selective hydrogenation of nitrobenzene to cyclohexanone oxime in the presence of NH2OH·HCl: Influence of the operative variables and insights on the reaction mechanism

Luca Pietrobon;
2020-01-01

Abstract

We studied the influence of temperature, solvent, pressure, catalysts type on the selectivity of nitrobenzenehydrogenation to cyclohexanone oxime (COX) in the presence of NH2OH. The best reaction conditions are:pressure 0.8 MPa, temperature 333 K, solvent ethers, and catalyst Pd/C5%. Other hydrogenation metal catalystsdid not give comparable results. The amount of Pd/C influences the yield in COX, which rises above to 90 % atthe highest load. The reaction profile shows that aniline is the reaction intermediate. Indeed, aniline as a sub-strate gives COX, though in lower yield than that achieved employing nitrobenzene. The NH2OH parallel hy-drogenation to NH4Cl, influences positively the selectivity to COX. It has been observed that COX, cyclohex-anone and N-cyclohexylideneaniline are in equilibrium in the reaction solution and all likely derive fromnucleophilic substitutions to a common imine intermediate formed on the Pd surface, whose high activity doesnot need any further metal catalyst
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2968379
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