(1R,3S,5R)-1,3,8-trimethyl-2,9-dioxabicyclo[3.3.1]non-7-en-6-one | 409313-32-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡喃
• 英文名称: (1R,3S,5R)-1,3,8-trimethyl-2,9-dioxabicyclo[3.3.1]non-7-en-6-one
• CAS: 409313-32-2
• 化学式: C₁₀H₁₄O₃
• 分子量: 182.219
• InChiKey: ZNKUBHOIUUERAD-FXBDTBDDSA-N

物化性质

• 沸点：
  271.7±40.0 °C(Predicted)
• 密度：
  1.102±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  13
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (1R,3S,5R)-1,3,8-trimethyl-2,9-dioxabicyclo[3.3.1]non-7-en-6-one 在 sodium tetrahydroborate 、 cerium(III) chloride 作用下， 以 甲醇 为溶剂， 反应 0.17h， 以94%的产率得到(1R,3S,5R,6R)-1,3,8-trimethyl-2,9-dioxabicyclo[3.3.1]non-7-en-6-ol
  参考文献：
  名称：

  Synthesis of (1R,3S,5S)-1,3,8-Trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene, the Male Pheromone of a Hepialid Moth, Endoclita excrescens, and Its Enantiomer

  摘要：

  The (1R,3S,5S)- and (1S,3R,5R)-isomers of 1,3,8-trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene were synthesized from the (S)- and (R)-isomers of ethyl 3-hydroxybutanoate. The (1 R,3S,5S)-isomer was identified as the pheromone produced by the male Japanese hepialid moth, Endoclita excrescens. ((C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

  DOI：

  10.1002/1099-0690(200212)2002:23<3974::aid-ejoc3974>3.0.co;2-z
• 作为产物：
  描述：

  (2R,6RS,2'S)-2-(2'-tert-butyldimethylsilyloxypropyl)-6-hydroxy-5,6-dimethyl-2H-pyran-3-one 在 氢氟酸 作用下， 以 乙腈 为溶剂， 反应 0.5h， 以79%的产率得到(1R,3S,5R)-1,3,8-trimethyl-2,9-dioxabicyclo[3.3.1]non-7-en-6-one
  参考文献：
  名称：

  Synthesis of (1R,3S,5S)-1,3,8-Trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene, the Male Pheromone of a Hepialid Moth, Endoclita excrescens, and Its Enantiomer

  摘要：

  The (1R,3S,5S)- and (1S,3R,5R)-isomers of 1,3,8-trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene were synthesized from the (S)- and (R)-isomers of ethyl 3-hydroxybutanoate. The (1 R,3S,5S)-isomer was identified as the pheromone produced by the male Japanese hepialid moth, Endoclita excrescens. ((C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

  DOI：

  10.1002/1099-0690(200212)2002:23<3974::aid-ejoc3974>3.0.co;2-z

文献信息

• Synthesis of (1R,3S,5S)-1,3,8-Trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene, the Male Pheromone of a Hepialid Moth, Endoclita excrescens, and Its Enantiomer
  作者：Kaoru Marukawa、Kenji Mori

  DOI：10.1002/1099-0690(200212)2002:23<3974::aid-ejoc3974>3.0.co;2-z

  日期：2002.12

  The (1R,3S,5S)- and (1S,3R,5R)-isomers of 1,3,8-trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene were synthesized from the (S)- and (R)-isomers of ethyl 3-hydroxybutanoate. The (1 R,3S,5S)-isomer was identified as the pheromone produced by the male Japanese hepialid moth, Endoclita excrescens. ((C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)