摘要
本文利用GC、GC/MS研究了通过2-氯-6-硝基甲苯(A)氯化制备α,α,2,6-四氯甲苯的反应过程。发现氯化首先在α-甲基上进行,生成α,2-二氯-6-硝基甲苯(B),B经硝基取代氯化(主要途径)生成α,2,6-三氯甲苯(C),C进一步发生α-氯代生成目的产物(D)。少量B还可经进一步的α-氯化形成α,α,2-三氯-6-硝基甲苯(E),E进一步发生硝基的氯取代而形成D。
The chlorination mechanism of 2 chloro 6 nitrotoluene(A) to α,α ,2,6 tetrachlorotoluene(D) has been studied by CM/MS.It is found that Cl attacks α H of A at first with the formation of an intermediate, α ,2 dichloro 6 nitro toluene (B) which turns subsequently to α ,2,6 trichlorotoluene(C) through denitrochlorination.C is then chlorinated on α H and forms D.Only a small amount of B is found to occure through another route to D,i.e.,via α,α ,2 trichloro 6 nitrotoluene(E) Ipso chlo rination to give 1,2,3 trichlorobnezene is also found to take place in the process.
出处
《化学研究与应用》
CAS
CSCD
1996年第4期484-488,共5页
Chemical Research and Application
关键词
氯化
四氯甲苯
色谱
质谱
chlorination, α,α ,2,6 tetrachlorotoluene,GC/MS