ethyl (4-phenylcyclohexen-1-yl)acetate | 143589-31-5

• 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: ethyl (4-phenylcyclohexen-1-yl)acetate
• 英文别名: (4-phenyl-cyclohex-1-enyl)-acetic acid ethyl ester；(4-Phenyl-cyclohex-1-enyl)-essigsaeure-aethylester；Ethyl 2-(4-phenylcyclohexen-1-yl)acetate
• CAS: 143589-31-5
• 化学式: C₁₆H₂₀O₂
• 分子量: 244.334
• InChiKey: MACIHHZMEZHQIW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  18
• 可旋转键数：
  5
• 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：

  溴乙酸乙酯 、 alkaline earth salt of/the/ methylsulfuric acid 在 锌 、 苯 作用下， 生成 ethyl (4-phenylcyclohexen-1-yl)acetate
  参考文献：
  名称：

  Fieser et al., Journal of the American Chemical Society, 1948, vol. 70, p. 3177

  摘要：

  DOI：

文献信息

• Microwave-assisted regioselective olefinations of cyclic mono- and di-ketones with a stabilized phosphorus ylide
  作者：Jinlong Wu、Dan Li、Huafeng Wu、Lijie Sun、Wei-Min Dai

  DOI：10.1016/j.tet.2005.12.060

  日期：2006.5

  4-cyclohexanediones with the ylide at 190 °C for 20 min in MeCN afforded the exocyclic olefins in >94:6 isomer ratios. On the other hand, the same reactions carried out at 230 °C for 20 min in the presence of 20 mol % DBU furnished the endocyclic olefins in >83:17 isomer ratios. The base-mediated isomerization of the exocyclic olefins into the endocyclic isomers was primarily driven by thermodynamic stability of the

  在控制的微波加热下，许多环状的单酮和二酮与（carbethoxyethidene）三苯基磷芳烷进行区域选择性烯烃化反应。4-取代的环己酮或1,2-和1,4-环己二酮与ylide在MeCN中在190°C下进行Wittig反应20分钟，得到的外环烯烃的异构体比率> 94：6。另一方面，在20mol％DBU的存在下在230℃下进行20分钟的相同反应提供了＞ 83:17异构体比率的内环烯烃。碱介导的环外烯烃异构化成环内异构体主要是由产物的热力学稳定性驱动的，并且研​​究了环结构对去共轭作用的影响。
• A Microwave-assisted Deconjugative Esterification of α,β-Unsaturated Carboxylic Acids through α,β-Unsaturated Ketene Intermediates
  作者：Shigeki Sano、Takashi Ichikawa、Michiyasu Nakao、Yoshimitsu Nagao

  DOI：10.1246/cl.2012.68

  日期：2012.1.5

  A facile synthetic approach to β,γ-unsaturated esters by deconjugative esterification of α,β-unsaturated carboxylic acids with alcohols in the presence of 1,3-dicyclohexylcarbodiimide (DCC), Me3N·HCl, and Me2NEt is described. The one-pot synthesis was effectively improved under microwave irradiation.

  一种简便的合成方法，通过在1,3-二环己基氨基脲（DCC）、氯化三甲胺（Me3N·HCl）和二乙基氨（Me2NEt）的存在下，将α,β-不饱和羧酸与醇进行脱共轭醇酯化，合成β,γ-不饱和酯。这种一步法合成在微波辐射下得到了有效改善。
• Novel Deconjugative Esterification of 2-Cyclohexylideneacetic Acids through 4-(Pyrrolidin-1-yl)pyridine-catalyzed Carbodiimide Couplings
  作者：Shigeki Sano、Etsuko Harada、Tomohiro Azetsu、Takashi Ichikawa、Michiyasu Nakao、Yoshimitsu Nagao

  DOI：10.1246/cl.2006.1286

  日期：2006.11

  4-(Pyrrolidin-1-yl)pyridine-catalyzed deconjugative esterification of 2-cyclohexylideneacetic acids afforded isopropyl 2-(cyclohex-1-enyl)acetate by employing 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride as a coupling reagent. On the other hand, 4-(pyrrolidin-1-yl)pyridine-catalyzed esterification with 1,3-dicyclohexylcarbodiimide was not accompanied by deconjugation and gave isopropyl 2-cyclohexylideneacetate.

  以 1-乙基-3-(3-二甲基氨基丙基)碳二亚胺盐酸盐为偶联试剂，4-(吡咯烷-1-基)吡啶催化的 2-环己基亚基乙酸脱共轭酯化反应生成了 2-(环己-1-烯基)乙酸异丙酯。另一方面，4-(吡咯烷-1-基)吡啶与 1,3-二环己基碳二亚胺催化的酯化反应不伴有解结合，得到 2-环己基亚基乙酸异丙酯。
• Highly regioselective Wittig reactions of cyclic ketones with a stabilized phosphorus ylide under controlled microwave heating
  作者：Jinlong Wu、Huafeng Wu、Shaoyong Wei、Wei-Min Dai

  DOI：10.1016/j.tetlet.2004.03.198

  日期：2004.5

  Significant base and temperature effects on the Wittig reactions of cyclohexanones with (carbethoxymethylene)triphenylphosphorane under microwave irradiation were observed. For the Wittig reactions carried out in a domestic microwave oven under solvent-free conditions, the initially formed exo-olefin products isomerized into the thermodynamically more stable endo-olefins due to uncontrolled high reaction temperature. In sharp contrast, under controlled microwave heating, both exo- and endo-olefins have been selectively synthesized by accurately regulating the reaction temperature with or without a base. (C) 2004 Elsevier Ltd. All rights reserved.
• Fieser et al., Journal of the American Chemical Society, 1948, vol. 70, p. 3177
  作者：Fieser et al.

  DOI：——

  日期：——