第 48 卷第 5 期 | | Vol. 48 No. 5 | 2018 年 10 月 | Oct 2018 |
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所属栏目:功能材料
续法合成N,N,N,N-四苄基环烯 |
杨学军,杜渭松,高嫒嫒,别国军,张严伟,黄劳劳,陈少青
(西安彩晶光电科技股份有限公司,陕西 西安 710065) |
摘 要:以乙醇胺、氯化苄为原料,经过N-苄基乙醇胺、N-苄基乙醇胺磺酸酯、N-苄基氮丙啶等中间体的合成,连续法合成医药中间体N,N',N'',N'''-四苄基环烯,其结构经IR、1H NMR、13C NMR和HRMS确证。中间体无需分离及纯化处理,4步反应总收率35.5%,高于文献收率。 |
关键词:N,N',N'',N'''-四苄基环烯;N-苄基氮丙啶;N-苄基乙醇胺磺酸酯;N-苄基乙醇胺;连续法 |
中图分类号:TQ463+.4 文献标识码:A 文章编号:1009-9212(2018)05-0055-04 |
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Synthesis of N,N',N'',N'''-Tetrabenzylcyclene by Continuous Method |
YANG Xue-jun, DU Wei-song, GAO Ai-ai, BIE Guo-jun, ZHANG Yan-wei, HUANG Lao-lao, CHEN Shao-qing
(Xi'an Caijing Opto-Electrical Science&Technology Co., Ltd., Xi'an 710065, China) |
Abstract:Using ethanolamine and benzyl chloride as the raw materials, the pharmaceutical intermediate N,N',N'',N'''-tetrabenzylcyclene was synthesized in a four-step continuous reaction, the product structure was confirmed by IR, 1H NMR, 13C NMR and HRMS. There was no requirement for separation and purification of the intermediates including N-benzylethanolamine, N-benzylethanolamine sulfonate and N-benzylethanolamine. A total yield of the whole four steps reaction was up to 35.5%. |
Key words:N,N',N'',N'''-tetrabenzylcyclene; N-benzylaziridine; N-benzylethanolamine sulfonate; N-benzylethanolamine; continuous process |
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作者简介:杨学军(1984-),男,甘肃会宁人,工程师,主要从事液晶显示材料、OLED显示材料及医药中间体的研发和生产工作(E-mail:yxj_19840@163.com)。
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收稿日期:2018-10-22
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