(1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol | 849065-24-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: (1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol
• 英文别名: (1R,2R,5S)-2-Azido-2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-ol；(1R,2R,5S)-2-azido-2-methyl-5-prop-1-en-2-ylcyclohexan-1-ol
• CAS: 849065-24-3
• 化学式: C₁₀H₁₇N₃O
• 分子量: 195.264
• InChiKey: ZIRZULKNFAGGAD-IVZWLZJFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  34.6
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol 在 三苯基膦 作用下， 以 1,4-二氧六环 为溶剂， 反应 24.0h， 以77%的产率得到(1R,4S,6S)-4-isopropenyl-1-methyl-7-azabicyclo-[4.1.0]heptane
  参考文献：
  名称：

  A convenient synthesis of new diamine, amino alcohol and aminophosphines chiral auxiliaries based on limonene oxide

  摘要：

  A strategy for the synthesis of new chiral auxiliaries based upon vicinal diamines, amino alcohols and aminophosphines, obtained from limonene oxide, has been developed. The methodology allows the preparation of (1R,2R,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohexane-1,2-diamine starting from a commercially available mixture of cis/trans (4S)-(-)-limonene oxides, through a stereoconvergent synthetic sequence. The process starts from an inexpensive naturally occurring material, is amenable to scale-up and allows easy access to highly useful enantiopure building blocks and ligands, employed in asymmetric catalysis. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2009.08.012
• 作为产物：
  描述：

  (−)-氧化柠檬烯（顺反异构体混合物） 在 sodium azide 、 氯化铵 作用下， 以 甲醇 为溶剂， 反应 24.0h， 生成 (1R,2R,5S)-2-azido-2-methyl-5-(prop-1-en-2-yl)cyclohexanol 、 (1R,2R,4S)-2-azido-1-methyl-4-(prop-1-en-2-yl)cyclohexanol
  参考文献：
  名称：

  Scaleable Syntheses of Isomeric Limonene Aziridines from the Commercially Available Mixture of cis- and trans-Limonene Oxides

  摘要：

  A short and efficient route to both isomers of limonene aziridine is described. The process is amenable to scale-up and allows easy access to multigram quantities of these highly useful chiral building blocks.

  DOI：

  10.1021/op0498464