2,3,3',4,6-penta-O-benzylsucrose | 302905-28-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2,3,3',4,6-penta-O-benzylsucrose
• CAS: 302905-28-8
• 化学式: C₄₇H₅₂O₁₁
• 分子量: 792.923
• InChiKey: NABGNRDLQXMXER-UGSLPANNSA-N

物化性质

• 沸点：
  890.7±65.0 °C(Predicted)
• 密度：
  1.30±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.73
• 重原子数：
  58.0
• 可旋转键数：
  20.0
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  134.53
• 氢给体数：
  3.0
• 氢受体数：
  11.0

反应信息

• 作为反应物：
  描述：

  2,3,3',4,6-penta-O-benzylsucrose 在 palladium on activated charcoal Amberlite IR-45(OH-) 、 氢气 作用下， 以 甲醇 、 乙酸乙酯 为溶剂， 以100%的产率得到蔗糖
  参考文献：
  名称：

  A Novel β-Directing Fructofuranosyl Donor Concept. Stereospecific Synthesis of Sucrose

  摘要：

  A new concept for the construction of beta-D-fructofuranosides based on the idea of locking the anomeric CH2OH group to the alpha-side through an internal bridge to the 4-hydroxyl group is presented. Thioglycoside fructose donors containing an internal 1,4-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl) (TIPS) acetal bridge have been constructed and used in glycosylations with dimethyl(thiomethyl)sulfonium triflate (DMTST) as promoter. The couplings were stereospecific to give beta-D-fructofuranosyl disaccharides in high yields. Using this approach, sucrose has been synthesized stereospecifically in 80% yield.

  DOI：

  10.1021/ja001439u
• 作为产物：
  描述：

  2,3,4,6-四-o-苄基-D-吡喃葡萄糖 在 di-tert-butylmethylpyridine 、 DMTST 、 tris(dimethylamino)sulfonium trimethylsilyldifluoride 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 3.0h， 生成 2,3,3',4,6-penta-O-benzylsucrose
  参考文献：
  名称：

  A Novel β-Directing Fructofuranosyl Donor Concept. Stereospecific Synthesis of Sucrose

  摘要：

  A new concept for the construction of beta-D-fructofuranosides based on the idea of locking the anomeric CH2OH group to the alpha-side through an internal bridge to the 4-hydroxyl group is presented. Thioglycoside fructose donors containing an internal 1,4-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl) (TIPS) acetal bridge have been constructed and used in glycosylations with dimethyl(thiomethyl)sulfonium triflate (DMTST) as promoter. The couplings were stereospecific to give beta-D-fructofuranosyl disaccharides in high yields. Using this approach, sucrose has been synthesized stereospecifically in 80% yield.

  DOI：

  10.1021/ja001439u