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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >MECHANISTIC ASPECTS OF THE MILD-CONDITION PHTHALIMIDINE SYNTHESIS WITH USE OF 1,2,3-1H-BENZOTRIAZOLE AND 2-MERCAPTOETHANOL AS DUAL SYNTHETIC AUXILIARIES
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MECHANISTIC ASPECTS OF THE MILD-CONDITION PHTHALIMIDINE SYNTHESIS WITH USE OF 1,2,3-1H-BENZOTRIAZOLE AND 2-MERCAPTOETHANOL AS DUAL SYNTHETIC AUXILIARIES

机译:使用1,2,3-1H-苯并三唑和2-巯基乙醇作为双重合成助剂的轻度邻苯二甲酰胺合成机理

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摘要

The mild-condition phthalimidine synthesis based on Mannich-type condensation reaction between o-phthalaldehyde and p-toluidine was first achieved with use of 1,2,3-1H-benzotriazole (Bt-H) and 2-mercaptoethanol (MET) as dual synthetic auxiliaries. Mechanistic aspects based on reaction condition optimization exercises are described.
机译:首先使用1,2,3-1H-苯并三唑(Bt-H)和2-巯基乙醇(MET)作为双重溶剂,基于邻苯二甲醛和对甲苯胺之间曼尼希式缩合反应的温和条件合成邻苯二甲酰亚胺合成助剂。描述了基于反应条件优化练习的机械方面。

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