(5α,6β,9α)-5,6,7,8,9,10-Hexahydro-2-hydroxy-6,10,10-trimethyl-5,9-methanobenzocyclooctene

• 分子结构分类: 有机化合物 - 苯类化合物 - 四氢化萘
• 英文名称: (5α,6β,9α)-5,6,7,8,9,10-Hexahydro-2-hydroxy-6,10,10-trimethyl-5,9-methanobenzocyclooctene
• 英文别名: (1R,9R,12R)-8,8,12-trimethyltricyclo[7.3.1.02,7]trideca-2(7),3,5-trien-5-ol
• 化学式: C₁₆H₂₂O
• 分子量: 230.35
• InChiKey: AHOZGNSLLRFQTF-JTNHKYCSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  17
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  (1α,3α,4β)-4-<1-<3-(4-Hydroxyphenyl)-4-methylcyclohexyl>-1-methylethyl>phenol 在 Amberlite 118 苯酚 作用下， 反应 96.0h， 生成 (5α,6β,9α)-5,6,7,8,9,10-Hexahydro-2-hydroxy-6,10,10-trimethyl-5,9-methanobenzocyclooctene
  参考文献：
  名称：

  Products from the Acid-Catalyzed Reaction of Cyclic Monoterpenes and Phenol

  摘要：

  Nine phenol-containing products from the acid-catalyzed reaction of phenol and gamma-terpinene were isolated and identified. A combination of X-ray crystallographic and spectroscopic techniques was used to assign the structures of the three p,p-bisphenols, two og-bisphenols, two bicyclic monophenols, and two bicyclic phenyl ethers. Several of the individual reaction products interconverted under acid-catalyzed conditions. The same nine products were formed using 3-carene, alpha-pinene, Limonene, or sabinene in place of gamma-terpinene, although the relative concentrations of these products varied depending upon the starting monoterpene's structure. A mechanism is proposed which accounts for the products' structures and reactivities.

  DOI：

  10.1021/jo00117a009