(Z)-cyclooct-2-en-1-yl 4-methylbenzoate

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (Z)-cyclooct-2-en-1-yl 4-methylbenzoate
• 英文别名: [(2Z)-cyclooct-2-en-1-yl] 4-methylbenzoate
• 化学式: C₁₆H₂₀O₂
• 分子量: 244.334
• InChiKey: OCUWZVBCMQRXIT-ALCCZGGFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  环辛烷 、 对二甲苯 、 copper diacetate 在 叔丁基过氧化氢 作用下， 反应 24.0h， 以11%的产率得到(Z)-cyclooct-2-en-1-yl 4-methylbenzoate
  参考文献：
  名称：

  Copper-Catalyzed Esterification of Alkylbenzenes with Cyclic Ethers and Cycloalkanes via C(sp³)–H Activation Following Cross-Dehydrogenative Coupling

  摘要：

  A copper-catalyzed cross-dehydrogenative coupling strategy has been developed for the synthesis of two classes of esters from simple solvents. The reaction of methylarenes with cyclic ethers resulted in alpha-acyloxy ethers involving four sp(3) C-H cleavages, while treatment of methylarenes with cycloalkanes led to the formation of allyl esters at the expense of six consecutive sp(3) C-H bonds.

  DOI：

  10.1021/ol5011906

文献信息

• Copper-Catalyzed Esterification of Alkylbenzenes with Cyclic Ethers and Cycloalkanes via C(sp³)–H Activation Following Cross-Dehydrogenative Coupling
  作者：Saroj Kumar Rout、Srimanta Guin、Wajid Ali、Anupal Gogoi、Bhisma K. Patel

  DOI：10.1021/ol5011906

  日期：2014.6.6

  A copper-catalyzed cross-dehydrogenative coupling strategy has been developed for the synthesis of two classes of esters from simple solvents. The reaction of methylarenes with cyclic ethers resulted in alpha-acyloxy ethers involving four sp(3) C-H cleavages, while treatment of methylarenes with cycloalkanes led to the formation of allyl esters at the expense of six consecutive sp(3) C-H bonds.