1976
DOI: 10.1002/chin.197603105
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ChemInform Abstract: KINETICS AND DIRECTION OF THE REDUCTION OF CHLORONITROBENZENES ON RANEY NICKEL

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“…In stud ies 23,24 , u p o n r e d u c t i o n o f chloronitrobenzene to Ni-skeleton, 5% Ir/C, the main inter mediate of the reaction was chlorophenylhydroxylamine. The adsorptive capacity of the starting compound is higher than that of chlorophenylhydroxylamine, so the authors suggested that, while there is chloronitrobenzene on the surface of the catalyst, phenylhydroxylamine accumulates in the reaction mixture without further conversion to chloroaniline.…”
Section: Experimental Study Of the Mechanism Of Nitro Compounds Reduction Haber-lukashevich' Mechanism Ideas Of V P Shmoninamentioning
confidence: 99%
“…In stud ies 23,24 , u p o n r e d u c t i o n o f chloronitrobenzene to Ni-skeleton, 5% Ir/C, the main inter mediate of the reaction was chlorophenylhydroxylamine. The adsorptive capacity of the starting compound is higher than that of chlorophenylhydroxylamine, so the authors suggested that, while there is chloronitrobenzene on the surface of the catalyst, phenylhydroxylamine accumulates in the reaction mixture without further conversion to chloroaniline.…”
Section: Experimental Study Of the Mechanism Of Nitro Compounds Reduction Haber-lukashevich' Mechanism Ideas Of V P Shmoninamentioning
confidence: 99%