FOOD SCIENCE ›› 2009, Vol. 30 ›› Issue (14 ): 153-155.doi: 10.7506/spkx1002-6630-200914027

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Iodine-Catalyzed Reaction of D-Glucose with Aceton for the Preparation of 1,2-5,6-di-O-Isopropylidene-alpha -Dglucofuranose (DAG)

HAN Xing-qian,HE Ji-guo*,CHEN Shang-wu,LI Bo   

  1. College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China
  • Received:2009-04-14 Online:2009-07-15 Published:2010-12-29
  • Contact: HE Ji-guo*, E-mail:hejiguo0870@sina.com

Abstract:

1,2-5,6-di-O-Isopropylidene-a-D-glucofuranose (DAG), a glucose derivative, was obtained by the reaction of Dglucose 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

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