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通过高效逆流色谱法从一锅合成中纯化和厚朴酚衍生物。

Purification of honokiol derivatives from one-pot synthesis by high-performance counter-current chromatography.

机构信息

State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Gaopeng Street, Keyuan Road 4, Chengdu 610041, China.

出版信息

J Chromatogr A. 2010 May 14;1217(20):3461-5. doi: 10.1016/j.chroma.2010.03.017. Epub 2010 Mar 18.

Abstract

This paper describes the application of high-performance counter-current chromatography (HPCCC) as a fast, useful and economic alternative for the separation and purification of seven honokiol derivatives (two of them are isomers), which were synthesized by a one-pot procedure. Five honokiol derivatives were successfully separated by n-hexane-ethyl acetate-methanol-water solvent system at three different volume ratios in a step-gradient elution. Two derivatives were obtained through a cycle elution mode. The whole separation process produced 366.3 mg, 323.6 mg, 242.8 mg, 216.2 mg, 203.5 mg, 185.8 mg and 279.3 mg of 3'-formylhonokiol (1), 2'-methoxy-3'-formylhonokiol (2), 2'-methoxyhonokiol (3), 4-methoxyhonokiol (4), 3',5-diformylhonokiol (5), 2',4-dimethoxy-3'-formylhonokiol (6) and 2',4-dimethoxyhonokiol (7) from crude sample of 3 g with purities of 98.7%, 99.3%, 98.6%, 98.2%, 99.0%, 98.4% and 99.2%, respectively. The purities and structural identification were determined by HPLC, (1)H NMR, (13)C NMR and mass spectroscopy.

摘要

本文描述了高效逆流色谱 (HPCCC) 在分离和纯化由一锅法合成的七种和厚朴酚衍生物(其中两种为异构体)中的应用。通过在三种不同体积比的正己烷-乙酸乙酯-甲醇-水溶剂系统中进行分步梯度洗脱,成功分离出五种和厚朴酚衍生物。两种衍生物通过循环洗脱模式获得。整个分离过程从 3 克粗样品中分别得到 366.3mg、323.6mg、242.8mg、216.2mg、203.5mg、185.8mg 和 279.3mg 的 3'-甲酰基和厚朴酚(1)、2'-甲氧基-3'-甲酰基和厚朴酚(2)、2'-甲氧基和厚朴酚(3)、4-甲氧基和厚朴酚(4)、3',5-二甲酰基和厚朴酚(5)、2',4-二甲氧基-3'-甲酰基和厚朴酚(6)和 2',4-二甲氧基和厚朴酚(7),纯度分别为 98.7%、99.3%、98.6%、98.2%、99.0%、98.4%和 99.2%。纯度和结构鉴定通过 HPLC、(1)H NMR、(13)C NMR 和质谱确定。

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