2-甲基-6-乙基-N-丁氧甲基-N-氯乙酰基苯胺的合成  

A New Process for Synthesis of 2-Methyl-6-ethyl-N-(butoxymethyl)-N-(chloroacetyl)aniline

作　　者：秦瑞香[1] 于世涛[1] 刘福胜[1] 解从霞[1] 

机构地区：[1]青岛科技大学化工学院,山东青岛266042

出　　处：《精细化工》2004年第z1期153-156,共4页Fine Chemicals

摘　　要：以2 甲基 6 乙基苯胺、甲醛、氯乙酰氯和正丁醇等为主要原料,以一种经济环保的工艺路线合成了杀菌剂2 甲基 6 乙基 N 丁氧甲基 N 氯乙酰基苯胺。考察了反应条件对反应结果的影响,获得了较佳的反应条件:烯胺化反应中n(甲醛)/n(2 甲基 6 乙基苯胺)=1 5,反应温度70～75℃,反应时间2h;酰化反应中n(氯乙酰氯)/n(2 甲基 6 乙基苯胺)=1 15,反应温度30～35℃,反应时间1 0h;醚化反应中n(丁醇)/n(2 甲基 6 乙基苯胺)=5 5,反应温度50℃,反应时间5h。在较佳反应条件下,产品质量分数和收率分别达到93%和90%。A new process for the synthesis of 2-methyl-6-ethyl-N-(butoxymethyl)-N-(chloroacetyl)aniline was studied using formaldehyde,2-methyl-6-ethylaniline,chloroacetyl chloride and butanol as starting materials.In the first step(N-methylenation),n(formaldehyde)/n(2-methyl-6-ethylaniline)=1.5,the reaction temperature is 70～75 ℃,and the reaction time is about 2 h.In the second step(acylation),n(chloroacetyl chloride)/n(2-methyl-6-ethylaniline)=1.15,the reaction temperature is 30～35 ℃,and the reaction time is about 1 h.In the third step(etherification),n(butanol)/n(2-methyl-6-ethylaniline)=5.5,the reaction temperature is 50 ℃,and the reaction time is about 5 h.Under these optimum reaction conditions,the purity and yield of the product were about 93% and 90% respectively.

关 键 词：杀菌剂 2-甲基-6-乙基-N-丁氧甲基-N-氯乙酰基苯胺 2-甲基-6-乙基苯胺 

分 类 号：TQ457[化学工程—农药化工]