New Method for Synthesis of 3-(4-hydroxy-3-methoxyphenyl) prop-2-enoic acid and 1-feruloyl-beta-D-glucose

被引:0
|
作者
Gokhale, Kunal M. [1 ]
机构
[1] Dr LH Hiranandani Coll Pharm, Pharm, Smt CHM Campus,Opposite Railway Stn, Ulhasnagar 421003, Maharashtra, India
关键词
Ferulic acid; 3-(4-hydroxy-3-methoxy phenyl) prop-2-enoic acid; tert-Butylhypohalite; Cu(I) CN; 1-Feruloyl-beta-D-glucose;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ferulic acid and its esters with polyhydroxy compounds have been tested for LDL-Cholesterol lowering, tumor suppressor activities and also have chemopreventive role in development of cancer. The conventional methods to obtain Ferulic acid [3-(4-hydroxy-3-methoxy phenyl) prop-2-enoic acid], a member of caffeic acid family, from natural resources are expensive whereas available synthetic methods suffer from limitations like long reaction time and low yield. 3-(4-hydroxy-3-methoxy phenyl) prop-2-enoic was synthesized using Cu(I) CN and tert-butylhypohalite with better yield. The reaction was carried out at ambient temperature and also involves simple work up. 1Feruloyl-beta-D-glucose, a substrate for serine carboxypeptidases was also synthesized with overall yield of 85%.
引用
收藏
页码:17 / 22
页数:6
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