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吉非罗齐的合成
引用本文:芦金荣,马英.吉非罗齐的合成[J].中国现代应用药学,2000,17(2):124-125.
作者姓名:芦金荣  马英
作者单位:1. 中国药科大学有机化学教研室,南京,210009
2. 浙江省医药学校,宁波,315010
摘    要:目的:合成吉非罗齐,并进行工艺改进。方法以2,5-二甲基苯酚为起始原料,与1-氯-3-溴丙烷反应,得3-(2,5-二甲基苯氧基)-1-氯丙烷,再与异丁酸钠锂作用,制得吉非罗齐。结果:通过两步反应制得产物,总收率43.8%,醚化反应经优化后收率较文献提高30%以上。合成产物经红外光谱,核磁共振谱及质谱确证。结论:缩短了反应步骤,提高了反应收率。

关 键 词:吉非罗齐  正丁基锂  合成  降血脂药  二甲基苯酚

Synthesis of gemfibrozil
Lu Jinrong.Synthesis of gemfibrozil[J].The Chinese Journal of Modern Applied Pharmacy,2000,17(2):124-125.
Authors:Lu Jinrong
Abstract:OBJECTIVE:To synthesize gemfibrozil and optimize the process.METHOD:Gemfibrozil was synthesized from 3 (2,5 xylyloxyl) propyl chloride which was reacted with sodium isobutyrate first and then react with n butyllithium.3 (2,5 xylyloxyl) propyl chloride was prepared from 2,5 dimethylphenol reacting with 1 bromo 3 chloropropane.RESULTS:Gemfibrozil was synthesized in two steps with the overall yield of 43.8%.The yield of etherification increased by 30% or more as compared with that in literature.The chemical structure of synthetic product were confirmed by IR, 1HNMR,MS.CONCLUSION:The synthetic route was simplized and the overall yield was raised.
Keywords:gemfibrozil  n-butyllithium  synthesis
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