PDF全文下载:2017010019
李秀芬,黄龙江,滕大为*
(青岛科技大学 化工学院,山东 青岛266042)
摘要:以三溴新戊醇为原料,经与对甲苯磺酰胺环合、环醚开环、羟基活化、环合等4步反应以58%的收率合成了目标产物,相比已有合成方法,该合成路线以甲磺酰基(-OMs)离去基替代溴原子,提高了收率、简化了反应的操作和后处理,适合工业化生产。
关键词:三溴新戊醇;2,6-二氮杂螺[3,3]庚烷; 合成
中图分类号:O 062文献标志码:A
引用格式:李秀芬,黄龙江,滕大为.2-苄基-6-对甲苯磺酰基-2,6-二氮杂螺[3,3]庚烷的合成[J].青岛科技大学学报(自然科学版), 2017, 38(1): 1923.
LI Xiufen, HUANG Longjiang, TENG Dawei.Synthesis of 2benzyl6tosyl2,6diazaspiro[3,3]heptane[J].Journal of Qingdao University of Science and Technology(Natural Science Edition), 2017, 38(1): 1923.
Synthesis of 2-Benzyl-6-tosyl-2,6-diazaspiro[3,3]heptane
LI Xiufen, HUANG Longjiang, TENG Dawei
(College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China)
Abstract: The 2-benzyl-6-tosyl-2,6-diazaspiro[3,3]heptane was synthesized by the reaction of cyzlization with p-toluenesulfonamide, ring opening of ether, activation of hydroxyl group and cycalization from pentaerythritol tribromide as raw material with 58% total yield. By using the methylsulfonyl group (-OMs) instead of Br, the mod-ified synthetic route is privileged with higher yield, more simple operation and especially suitable for industrial production.
Key words: pentaerythritol tribromide; 2,6-diazaspiro[3,3]heptanes; synthesis
收稿日期:20150828
基金项目:山东省自然科学基金项目(ZR2014BL028).
作者简介:李秀芬(1976—),女,讲师.*通信联系人.
文章编号:16726987(2017)01001905;DOI:10.16351/j.16726987.2017.01.003