6',8'-Dimethylenespiro3,7>octan>-4'-one | 155717-40-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 6',8'-Dimethylenespiro3,7>octan>-4'-one
• 英文别名: 6',8'-dimethylidenespiro[cyclopentane-1,4'-tricyclo[3.3.0.03,7]octane]-2'-one
• CAS: 155717-40-1
• 化学式: C₁₄H₁₆O
• 分子量: 200.28
• InChiKey: QKETXPULYYWMOY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  15
• 可旋转键数：
  0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  6',8'-Dimethylenespiro3,7>octan>-4'-one 以 氘代苯 为溶剂， 生成
  参考文献：
  名称：

  Synthesis and Properties of 2,4,6-Trimethylenetricyclo[3.3.0.03,7]octane (Stellatriene) and Its Alkyl Derivatives. Candidates for a Two-Step Cope Rearrangement

  摘要：

  The synthesis of 2,4,6-trimethylenetricyclo[3.3.0.0(3,7)] octane (stellatriene, 9), its hexamethyl derivative 37, and the spirocyclic derivatives 67 and 68, substituted at the carbon atom of the saturated bridge of the tricyclic system, are described. Key steps in the syntheses include an intramolecular Paterno-Buchi reaction leading to tetracyclic oxetanes (e.g., 22b, 39, 47, 59, and 60) as well as the cleavage of the oxetane ring induced by various bases. During the synthesis several dienones were prepared (35, 41, 50, 63, and 64). The trienes and the dienones rearrange to triquinane derivatives at temperatures between 25 and 50 degrees C. The half-lives of the molecules in solution have been determined, which indicate only a moderate effect of the methyl groups on the stability. The rearranged products can best be explained by assuming a stepwise Cope rearrangement via two allylic fragments.

  DOI：

  10.1021/jo00084a019
• 作为产物：
  描述：

  4,6-Diisopropylidenetricyclo<3.3.0.0^3,7>octan-2-ol 在 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 生成 6',8'-Dimethylenespiro3,7>octan>-4'-one
  参考文献：
  名称：

  Synthesis and Properties of 2,4,6-Trimethylenetricyclo[3.3.0.03,7]octane (Stellatriene) and Its Alkyl Derivatives. Candidates for a Two-Step Cope Rearrangement

  摘要：

  The synthesis of 2,4,6-trimethylenetricyclo[3.3.0.0(3,7)] octane (stellatriene, 9), its hexamethyl derivative 37, and the spirocyclic derivatives 67 and 68, substituted at the carbon atom of the saturated bridge of the tricyclic system, are described. Key steps in the syntheses include an intramolecular Paterno-Buchi reaction leading to tetracyclic oxetanes (e.g., 22b, 39, 47, 59, and 60) as well as the cleavage of the oxetane ring induced by various bases. During the synthesis several dienones were prepared (35, 41, 50, 63, and 64). The trienes and the dienones rearrange to triquinane derivatives at temperatures between 25 and 50 degrees C. The half-lives of the molecules in solution have been determined, which indicate only a moderate effect of the methyl groups on the stability. The rearranged products can best be explained by assuming a stepwise Cope rearrangement via two allylic fragments.

  DOI：

  10.1021/jo00084a019