张星星,胡志雄,贺军波,张维农,齐玉堂.月桂酸缩水甘油酯的相转移催化合成与表征[J].食品安全质量检测学报,2015,6(10):4103-4109
月桂酸缩水甘油酯的相转移催化合成与表征
Phase transfer catalytic synthesis and characterization of glycidyl laurate
投稿时间:2015-08-09  修订日期:2015-10-12
DOI:
中文关键词:  月桂酸缩水甘油酯  合成  纯化  表征
英文关键词:glycidyl laurate  synthesis  purification  characterization
基金项目:国家自然科学(31371783)、国家“十二五”科技支撑计划项目(2014BAD04B03)、国家粮食局公益性行业科研专项(2013007)、武汉轻工大学研究生教育创新计划项目(2014cx016)
作者单位
张星星 武汉轻工大学食品科学与工程学院 
胡志雄 武汉轻工大学食品科学与工程学院;农产品加工湖北省协同创新中心 
贺军波 武汉轻工大学食品科学与工程学院;农产品加工湖北省协同创新中心 
张维农 武汉轻工大学食品科学与工程学院;农产品加工湖北省协同创新中心 
齐玉堂 武汉轻工大学食品科学与工程学院 
AuthorInstitution
ZHANG Xing-Xing College of Food Science and Engineering,Wuhan Polytechnic University 
HU Zhi-Xiong College of Food Science and Engineering,Wuhan Polytechnic University;Hubei Collaborative Innovation Center for Processing of Agricultural Products, Wuhan 
HE Jun-Bo College of Food Science and Engineering,Wuhan Polytechnic University;Hubei Collaborative Innovation Center for Processing of Agricultural Products, Wuhan 
ZHANG Wei-Nong College of Food Science and Engineering,Wuhan Polytechnic University; Hubei Collaborative Innovation Center for Processing of Agricultural Products, Wuhan 
QI Yu-Tang College of Food Science and Engineering,Wuhan Polytechnic University 
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中文摘要:
      目的 旨在研究月桂酸缩水甘油酯的有效合成、纯化方法,为食用油脂中脂肪酸缩水甘油酯的检测提供相关对照品。方法 以月桂酸钠和环氧氯丙烷为起始原料,四丁基溴化铵为催化剂,采用相转催化法一步合成了月桂酸缩水甘油酯,通过甲醇/正己烷为萃取溶液及重结晶的方式得到纯品。纯化后的产物经高效液相、红外光谱、元素分析、质谱等手段进行表征。结果 产物经表征后确证为月桂酸缩水甘油酯,在优化条件下产物的纯度可达95%以上,符合标准对照品的纯度要求。结论 该方法以环氧氯丙烷为反应物和溶剂,原料易得、成本低廉,反应效率高、操作简便,为脂肪酸缩水甘油酯的合成提供了一种有效途径与方法。
英文摘要:
      Objective To study the effective synthesis and purification methods of glycidyl laurate and provide standard reference products for the detection of glycidyl fatty acid ester in edible oils and fats. Methods In this paper, glycidyl laurate has been synthesized by one-step phase transfer catalysis with sodium laurate (SL) and epichlorohydrin (ECH) as reactants and tetrabutyl ammonium bromide (TBAB) as catalyst, the resultant products were purified by liquid-liquid extraction with the mixture solvent of methanol and hexane, the residue of hexane layer was then recrystallized to prepare purified samples. The obtained products were characterized by high performance liquid chromatography (HPLC), infrared spectrum (IR), elemental analysis and mass spectrum (MS). Results The product was confirmed to be glycidyl laurate, and its purity could reach more than 95% under optimized conditions, which conformed to the required purity of standard reference material. Conclusion Epichlorohydrin was used as reactants and solvents in the phase transfer catalytic synthesis of glycidyl laurate, which will guarantee many advantages such as easily obtaining of raw materials, low cost, high efficiency and simple operation. Therefore, the proposed method will provide an effective approach for the synthesis of glycidyl fatty acid ester.
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