摘要
在强碱催化下,甲基异丙酮和4-氟苯甲醛通过羟醛缩合反应得到α,β-不饱和酮2,然后与苯甲醛生成1,4-二酮化合物,将其与醋酸铵在醋酸催化下一锅法得到吡咯化合物,最后在叔丁基锂强碱作用下,与苯基异氰酸酯反应得到目标产物吡咯羧酸苯基酰胺类化合物。
α,β-unsaturated ketone is synthesized by aldol reaction of 4-fluorobenzaldehyde and methyl isopropyl ketone in presence of 15%KOH solution,then it reacts with benzaldehyde again for generating 1,4-diketones compound,which reacts with NH4OAc under AcOH catalysis by one-pot synthesis and pyrrole compound is obtained.And finally,under the catalytic action of a strong base of tert-butyllithium,pyrrole compound react with isocyanato-benzene for the target product of phenylamide compounds of pyrrolidine carboxylate.
作者
匡仁云
郭瑾
谢宝星
KUANG Ren-yun;GUO Jing;XIE Bao-xing(School of Chemistry and Chemical Engineering,Jinggangshan University,Ji'an,Jiangxi 343009,China)
出处
《井冈山大学学报(自然科学版)》
2020年第6期15-17,共3页
Journal of Jinggangshan University (Natural Science)
基金
国家自然科学基金项目(21563015)。
关键词
羟醛缩合
吡咯衍生物
一锅法
合成
aldol reaction
pyrrole derivative
one-pot reaction
synthesis