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1—取代氮杂环庚烷—2—酮的合成
引用本文:周瑞仪,张洪奎.1—取代氮杂环庚烷—2—酮的合成[J].厦门大学学报(自然科学版),1990,29(5):596-598.
作者姓名:周瑞仪  张洪奎
作者单位:厦门大学化学系 (周瑞仪,张洪奎),厦门大学化学系(任海英)
摘    要:1—取代氮杂环庚烷-2-酮类有比较重要的生理活性,如1-十二烷基氮杂环庚烷-2-酮为目前受重视的新型高效、无毒的透皮吸收促进剂。但内酰胺氮上氢原子的酸性很弱,较难发生N-烷基化反应,为提高1-取代内酰胺的合成产率,我们用混合无机碱KOH/K_2CO_3为缚酸剂,聚

关 键 词:氮杂环庚烷酮  合成  N-烷基化

Studies on Synthesis of l-substituted Azacycloheptan-2-ones
Zhou Ruiyi Zhang Hongkui Ren Haiying Dept. of Chem..Studies on Synthesis of l-substituted Azacycloheptan-2-ones[J].Journal of Xiamen University(Natural Science),1990,29(5):596-598.
Authors:Zhou Ruiyi Zhang Hongkui Ren Haiying Dept of Chem
Institution:Zhou Ruiyi Zhang Hongkui Ren Haiying Dept. of Chem.
Abstract:1-substituted azacycloheptan-2-ones were synthesized by means of solid-liquid phase transfer catalysis of polyethylene glycol. In this PTC-alkylation we have found that a mixture of solid NaOH and K2C03as a base is more suitable for N-alkrlation of caprolactam. The procedure is simple to op eiate and inexpensive
Keywords:1-substituted azacycloheptan-2-ones  Phase transfer catalysis (PTC)  Polyethylene glycoi  N-alkylation  Caprolactam
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