碘催化的葡萄糖异亚丙基缩酮反应研究
※工艺技术 食品科学 2009, Vol. 30, No. 14 153
韩兴谦,何计国* ,陈尚武,李 博
( 中国农业大学食品科学与营养工程学院,北京 100083)
以无水葡萄糖为原料、碘为催化剂,催化无水葡萄糖与丙酮的异亚丙基缩酮反应,形成1,2-5,6- 双- 氧-
异丙叉- α-D- 呋喃葡萄糖(1,2-5,6-di-O-isopropylidene- α-D-glucofuranose ,diacetone glucose ,DAG) ,并对反应条
件进行初步研究。结果表明:碘做催化剂,在回流条件下,5h 能催化葡萄糖与丙酮生成产物DAG ;而在低于
回流温度反应时,反应时间明显变长。在反应物料最佳物质的量比为葡萄糖:碘:丙酮=1:0.15:122.5 时,最高收率为
75% 左右;4A 分子筛的加入并不能显著提高反应收率。
碘;1,2-5,6- 双- 氧- 异丙叉- α-D - 呋喃葡萄糖;丙酮;缩合反应
Iodine-Catalyzed Reaction of D-Glucose with Aceton for the Preparation of 1,2-5,6-di-O-Isopropylidene-alpha -D-
glucofuranose (DAG)
HAN Xing-qian ,HE Ji-guo* ,CHEN Shang-wu ,LI Bo
(College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China)
Abstract :1,2-5,6-di-O-Isopropylidene-a-D-glucofuranose (DAG), a glucose derivative, was obtained by the reaction of D-
glucose with acetone. Effects of various conditions such as temperature, D-glucose/iodine/acetone ratio (molar) and amount of
added 4A molecular sieve on production yield of DAG were investigated. In the presence of iodine, heating for 5 h under reflux
(at 62 ℃) allowed the generation of DAG from the reaction between D-glucose and acetone. However, the reaction time was greatly
extended when the reaction temperature was below 62 ℃. At optimized D-glucose/iodine/acetone ratio of 1:0.15:122.5, the yield
of DAG was found to be close to 75%. No obvious effect was found on the yield of DAG with the addition of 4A molecular sieve.
Key words :iodine ;1,2-5,6-di-O-isopropylidene-a-D -glucofuranose ;acetone ;condensation
中图分类号:TQ203.2 文献标识码:A 文章编号:1002-6630(2009)14-0153-03
1,2-5,6- 双- 氧- 异丙叉- α-D- 呋喃葡萄糖(1,2-5,6-di- 低;然而国外开发的一些新型催化剂、价格昂贵、不
O -isopropy
您可能关注的文档
最近下载
- DB31T 1104-2018 城市轨道交通导向标识系统设计规范.docx VIP
- GB50461-2024:石油化工静设备安装工程施工质量验收规范.pptx VIP
- 2023年浙江省军队转业干部录用考试试题.docx VIP
- 口渴了-朋友帮你.ppt VIP
- Xikong西莱克低温机控制板SHXK814用户手册.pdf
- 爱迪生牛顿大发明攻略.doc VIP
- 重庆天齐锂电新材料有限公司新建1000吨_年高能锂电材料电池级金属锂项目环评报告.pdf VIP
- 朗文3A复习资料及垃圾分类作文8篇.doc VIP
- DB65T 3694-2015 现行哈萨克文与西里尔哈萨克文编码字符转换规则.docx VIP
- 华为云服务登录.doc VIP
原创力文档

文档评论(0)