334. Reactions of aromatic nitro-compounds in alkaline media. Part V. Solutions of methyl picrate and 1,3,5-trinitrobenzene in aqueous sodium hydroxide in the absence of light

Author(s):  
V. Gold ◽  
C. H. Rochester
2014 ◽  
Vol 1033-1034 ◽  
pp. 18-21
Author(s):  
Ke Ying Cai ◽  
Ying Mei Zhou

The reduction of aromatic nitro compounds to corresponding azoxy compounds with sodium borohydride was catalyzed by BiO(OH)/actived carbon (AC), which was prepared by equivalent-volume impregnation. The influences of catalyst, sodium borohydride and sodium hydroxide amount were investigated with 10 mmol of nitrobenzene as substrate in methanol at room temperature. The suitable reaction conditions are as follows: 0.2 g of catalyst, 10 mmol of sodium borohydride and 0.1 g of sodium hydroxide. Under the conditions, the seven aromatic nitro compounds were reduced to corresponding azoxy compounds with 27%-90% yields. Moreover, slight deactivation was observed after nine cycles of the catalyst.


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