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抗倒酯的合成研究 被引量:1

Study on synthesis of trinexapac-ethyl
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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
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参考文献6

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二级参考文献10

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