摘要
以丙酮和马来酸二乙酯为原料,经过迈克尔加成、环合、酰化及重排反应合成了抗倒酯,4步反应总收率63.4%。中间体及产品经~1HNMR和质谱表征。该方法具有操作简单、成本低、收率高等优点,适合工业化生产。
Trinexapac-ethyl was synthesized by using acetone and diethyl maleate as the starting material via Michael addition,cyclization,acylation and rearrangement.The total yield of four steps was 63.4%.Structure of the product and intermediate was confirmed by ~1HNMR and MS.This method has many advantages,such as easy operation,low cost and high yield,which can be feasible to large scale preparation.
出处
《精细与专用化学品》
CAS
2011年第8期11-13,共3页
Fine and Specialty Chemicals
基金
2010年江苏省高等学校大学生实践创新训练计划立项项目(苏教高[2010]27号
编号60)
关键词
马来酸二乙酯
迈克尔加成
环合
酰化
重排
抗倒酯
diethyl maleate
Michael addition
cyclization
acylation
rearrangement
trinexapac-ethyl