摘要
基于(2R,3R)-1,1,4,4-四苯基丁四醇的区域选择性2,3-二甲基化反应,建立了一种制备C_2手性二醇即(2R,3R)-2,3-二甲氧基-1,1,4,4-四苯基-1,4-丁二醇的实用方法.结果表明:与文献相比,该合成避免了酸的使用,减少了多取代THF衍生物的生成,提高了产率,不仅是制备(2R,3R)-2,3-二甲氧基-1,1,4,4-四苯基-1,4-丁二醇的便捷方法,也为(2R,3R)-1,1,4,4-四取代丁四醇的区域选择性衍生化提供了重要信息.
A practical approach to(2R,3R)-2,3-dimethoxy-1,1,4,4-tetraphenylbutane-1,4-diol,a C2 chiral diol,was developed based on highly regioselective 2,3-methylation of(2R,3R)-1,1,4,4-tetraphenylbutaneol with MeI/NaH. The results indicated that compared with the literature,this procedure avoided the treatment with acid,reduced the generation of poly-substituted THF derivative,and increased the yield. This report not only provided a practical approach to prepare(2R,3R)-2,3-dimethoxy-1,1,4,4-tetraphenylbutane-1,4-diol,but also presented a significant reference for the regioselective derivatization of(2R,3R)-1,1,4,4-tetra-substituted butanetetraols.
作者
胡晓允
尹忠友
唐艳柳
吴腊梅
HU Xiaoyun;YIN Zhongyou;TANG Yanliu;WU Lamei(College of Chemistry and Materials,South-Central University for Nationalities,Wuhan 430074,China)
出处
《中南民族大学学报(自然科学版)》
CAS
2019年第1期22-26,共5页
Journal of South-Central University for Nationalities:Natural Science Edition
基金
国家自然科学基金资助项目(21302233)
湖北省自然科学基金资助项目(2012FFB07410)
中央高校基本科研业务费专项资金资助项目(CZY18010)
关键词
选择性甲基化
(2R
3R)-1
1
4
4-四苯基丁四醇
(2R
3R)-2
3-二甲氧基-1
1
4
4-四苯基-1
4-丁二醇
环醚化
selective methylation
(2R,3R)-1,1,4,4-tetraphenylbutaneol
(2R,3R)-2,3-dimethoxy-1,1,4,4tetraphenylbutane-1,4-diol
cycloetherization