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褪黑素合成及环化机理研究

Study of synthesize melatonin and cyclic reaction mechanism
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摘要 以邻苯二甲酰亚胺钾盐为起始原料,经五步反应合成了褪黑素,鉴定了产物结构,合成收率达35.6%,纯度99.1%。对中间产物2-羧乙酯基-3-(2-邻苯二甲酰亚胺乙基)-5-甲氧基-吲哚的环化反应过程进行了机理研究,为最佳工艺条件的确定提供了理论依据。 This paper reported synthesis of melatonin by five-step reaction route with K-phthalimide, the product was determined ,the overall yield is 35.6%, product purity over 99.1%. The paper studied the cyclic reaction mechanism of 2-ethoxycarbonyl-3- (2-phthalimidoethyl) -5-methoxy-indole, provided of theoretical for optimum condition.
出处 《应用化工》 CAS CSCD 2009年第2期243-247,共5页 Applied Chemical Industry
关键词 邻苯二甲酰亚胺钾盐 褪黑素 合成 2-羧乙酯基-3-(2-邻苯二甲酰亚胺乙基)-5-甲氧基-吲哚 环化机理 k-phthalimide melatonin synthesis 2-ethoxycarbonyl-3-(2-phthalimidoethyl) -5-methoxy-indole cyclic mechanism
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参考文献6

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