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两步法合成间硝基苯甲醛
Two Step Synthesis of m-Nitrobenzaldehyde
【摘要】 间硝基甲苯与双氧水、氢溴酸在AIBN作用下,生成间硝基一溴苄和二溴苄,再经DMSO、二甲胺氧化水解生成间硝基苯甲醛。研究了溴化、氧化水解反应的影响因素,优化了反应条件。结果表明,溴化反应较佳的条件为:溴化温度60℃,溴化时间4 h,n(间硝基甲苯)∶n(氢溴酸)∶n(双氧水)=1∶2.5∶2.5,AIBN用量0.8 g;氧化水解反应较佳的条件为:氧化温度105℃,保温时间8 h,水解温度60℃,水解时间1 h。在该条件下,间硝基苯甲醛收率达58.6%,色谱纯度达99.1%。通过IR和1HNMR对产物结构进行了表征。
【Abstract】 m-Nitrobenzyl bromide and 1-(dibromomethyl)-3-nitrobenzene,which were prepared with m-nitrotoluene,hydrogen peroxide and hydrobromic acid over AIBN,was oxided and hydrolyzed by DMSO and dimethylamine to produce m-nitrobenzaldehyde.Factors influencing bromination,hydrolysis and oxidization were investigated.The yield and purity of m-nitrobenzaldehyde are 58.6% and 99.1% respectively under the optimal bromination conditions:bromination temperature 60 ℃,bromination time 4 h,n(m-nitrotoluene)∶ n(HBr)∶ n(H2O2)=1∶ 2.5∶ 2.5,the amount of AIBN 0.8 g,and oxidization-hydrolysis conditions:oxidization temperature 105 ℃,heat preservation time 8 h,hydrolysis temperature 60 ℃,hydrolysis time 1 h.The structure of the product was identified by IR and 1HNMR.
【Key words】 m-nitrotoluene; m-nitrobenzaldehyde; bromination; oxidization and hydrolysis; dimethylamine; fine chemical intermediates;
- 【文献出处】 精细化工 ,Fine Chemicals , 编辑部邮箱 ,2011年02期
- 【分类号】TQ244.1
- 【被引频次】4
- 【下载频次】582