2-(4-hydroxybutyl)cyclohexanone | 51060-37-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-(4-hydroxybutyl)cyclohexanone
• 英文别名: 2-(4-hydroxybutyl)cyclohexan-1-one
• CAS: 51060-37-8
• 化学式: C₁₀H₁₈O₂
• 分子量: 170.252
• InChiKey: MJYLLIYTJVPTRE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  12
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(4-hydroxybutyl)cyclohexanone 在 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 生成 1-Oxo-2-(4-oxobutyl)-cyclohexan
  参考文献：
  名称：

  Intramolecular Anodic Olefin Coupling Reactions: A New Approach to the Synthesis of Angularly Fused, Tricyclic Enones

  摘要：

  A number of intramolecular anodic olefin coupling reactions have been examined in order to determine the feasibility of using a sequential electrochemical oxidation-aldol condensation approach for constructing polycyclic enones. Initially, substrates comprised of an aldehyde enol ether tethered to a ketone enol ether were examined. In a model study, it was shown that such a substrate could lead to a successful electrochemical oxidation-aldol condensation sequence. However, the difficulties associated with both the synthesis and the poor stability of the ketone enol ethers greatly reduced the potential utility of this approach. This problem was circumvented by taking advantage of the compatibility of allylsilane groups with the electrolysis reaction. In these examples, ozonolysis of the electrochemical cyclization product afforded the 1,4-dicarbonyl substrate needed for the aldol condensation. The use of the less reactive allylsilane group in the electrochemical reaction still allowed for the construction of quaternary carbons. Finally a pair of angularly fused, tricyclic enones were synthesized. The regiochemistry of the enone in the product could be controlled by the proper choice of the substrate for the electrolysis and manipulation of the resulting cyclized product.

  DOI：

  10.1021/jo00088a019
• 作为产物：
  描述：

  4-[(2E)-2-hydroxyiminocyclohexyl]butan-1-ol 以88%的产率得到
  参考文献：
  名称：

  VANKAR PADMA; RATHORE RAJENDRA; CHANDRASEKARAN SRINIVASAN, J. ORG. CHEM., 51,(1986) N 15, 3063-3065

  摘要：

  DOI：

文献信息

• Stereochemistry of intramolecular cyclopropanation of an organoiron reagent
  作者：Ramnath S. Iyer、Gee Hong Kuo、Paul Helquist

  DOI：10.1021/jo00350a102

  日期：1985.12
• A mild and highly selective method for the regeneration of carbonyl compounds from oximes and (2,4-dinitrophenyl)hydrazones
  作者：Padma Vankar、Rajendra Rathore、Srinivasan Chandrasekaran

  DOI：10.1021/jo00365a042

  日期：1986.7
• VANKAR PADMA; RATHORE RAJENDRA; CHANDRASEKARAN SRINIVASAN, J. ORG. CHEM., 51,(1986) N 15, 3063-3065
  作者：VANKAR PADMA、 RATHORE RAJENDRA、 CHANDRASEKARAN SRINIVASAN

  DOI：——

  日期：——
• Intramolecular Anodic Olefin Coupling Reactions: A New Approach to the Synthesis of Angularly Fused, Tricyclic Enones
  作者：Luzviminda V. Tinao-Wooldridge、Kevin D. Moeller、Christine M. Hudson

  DOI：10.1021/jo00088a019

  日期：1994.5

  A number of intramolecular anodic olefin coupling reactions have been examined in order to determine the feasibility of using a sequential electrochemical oxidation-aldol condensation approach for constructing polycyclic enones. Initially, substrates comprised of an aldehyde enol ether tethered to a ketone enol ether were examined. In a model study, it was shown that such a substrate could lead to a successful electrochemical oxidation-aldol condensation sequence. However, the difficulties associated with both the synthesis and the poor stability of the ketone enol ethers greatly reduced the potential utility of this approach. This problem was circumvented by taking advantage of the compatibility of allylsilane groups with the electrolysis reaction. In these examples, ozonolysis of the electrochemical cyclization product afforded the 1,4-dicarbonyl substrate needed for the aldol condensation. The use of the less reactive allylsilane group in the electrochemical reaction still allowed for the construction of quaternary carbons. Finally a pair of angularly fused, tricyclic enones were synthesized. The regiochemistry of the enone in the product could be controlled by the proper choice of the substrate for the electrolysis and manipulation of the resulting cyclized product.