摘要
文章以均三甲苯为原料,经过氧化、胺化和降解反应得到3,5-二甲基苯胺,重点研究了由3,5-二甲基苯甲酰胺霍夫曼降解制备3,5-二甲基苯胺的反应及由N-溴代-3,5-二甲基苯甲酰胺制备3,5-二甲基苯胺反应的动力学。结果表明,在降解反应中,当物料比n(3,5-二甲基苯甲酰胺):n(NaOH):n(Br2)=1:12.12:4.24,重排反应温度为0℃,水解温度为90—100℃,水解时间为1h,3,5-二甲基苯胺的收率较高,为45%;动力学反应活化能(Ea)为1.04×10^5J/mol。
With mesitylene as raw material, 3, 5-Dimethylaniline was prepared through reactions of oxidization, amination and Hofmann degradation. More attention was attached to the synthesis of 3, 5-dimethylaniline through Hofmann degradation from 3, 5-dimethylbenzamide and the kinetics of the reaction which 3, 5-dimethylaniline is prepared by N-bromo-3, 5-dimethylbenzamide. The results show the optimum conditions for Hofmann degradation are as follows: the ratio of 3, 5-dimethylbenzamide to sodium hydroxide and bromine is 1:12.12:4. 24, rearrangement reaction temperature is 0 ℃, hydrolysis reaction temperature is from 90 ℃ to 100 ℃ and reaction time is lh. The yield of 3, 5-dimethylaniline is 45%, and the activation energy of the kinetics is 1.04 × 10^5 J/molo
出处
《辽东学院学报(自然科学版)》
CAS
2010年第1期8-13,17,共7页
Journal of Eastern Liaoning University:Natural Science Edition