(E) and (Z)-4-cyclohexyl-3-buten-1-ol | 865444-41-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (E) and (Z)-4-cyclohexyl-3-buten-1-ol
• 英文别名: (E/Z)-4-cyclohexylbut-3-en-1-ol；4-Cyclohexylbut-3-en-1-ol
• CAS: 865444-41-3
• 化学式: C₁₀H₁₈O
• 分子量: 154.252
• InChiKey: YKKJHHKZYSPQEY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  11
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (E) and (Z)-4-cyclohexyl-3-buten-1-ol 在 三氟甲磺酸 、 dimethyl sulfide borane 、 sodium hydroxide 、 双氧水 作用下， 以 二氯甲烷 、 甲醇 、 水 为溶剂， 以80%的产率得到4-Cyclohexylbutane-1,3-diol
  参考文献：
  名称：

  Oxygen-Directed Intramolecular Hydroboration

  摘要：

  Metal-free homoallylic oxygen-directed intramolecular hydroboration is reported. Regioselectivities from 20:1 to 82:1 favoring the 1,3-dioxy-substituted products have been achieved using Me2S center dot BH3/TfOH followed by standard oxidative workup. Branching at the C5 position improves regioselectivity.

  DOI：

  10.1021/ja800402g
• 作为产物：
  描述：

  1-环己基-2-丙醇 在 4,4'-二叔丁基苯并 三甲基氯硅烷 、 lithium 作用下， 以 四氢呋喃 、 四氯化碳 为溶剂， 反应 3.0h， 生成 (E) and (Z)-4-cyclohexyl-3-buten-1-ol
  参考文献：
  名称：

  [2,3]-通过氯-锂交换进行的维蒂希重排

  摘要：

  不同的烯丙基氯甲基醚1与过量的锂粉（摩尔比为1：7）和催化量的DTBB（2.5 mol％）在THF中的反应在0°C下反应1 h，在用水水解后，得到预期的[2,3] -Wittig重排产生的唯一醇2。如对苄基氯甲基醚所举例说明的，相同的方法也可用于相应的[1,2]-维蒂希重排。

  DOI：

  10.1016/j.tetlet.2005.06.160

文献信息

• Application of Sulfuryl Chloride for the Quick Construction of β-Chlorotetrahydrofuran Derivatives from Homoallylic Alcohols under Mild Conditions
  作者：Wei Sun、Xianghua Zeng、Chengxia Miao、Shoufeng Wang、Chungu Xia

  DOI：10.1055/s-0033-1339351

  日期：——

  mild method is reported for the construction of β-chlorotetrahydrofuran derivatives by 5-endo chlorocycloetherification of homoallylic alcohols. The system employs sulfuryl chloride as the chlorinating agent under catalyst-free conditions. A variety of homoallylic alcohols with aryl or alkyl substituents were smoothly converted into β-chlorotetrahydrofurans in yields up to 98%. An efficient and mild method

  摘要 据报道，通过均烯丙基醇的5-内氯环醚化来构建β-氯四氢呋喃衍生物的有效而温和的方法。该系统在无催化剂的条件下采用磺酰氯作为氯化剂。各种具有芳基或烷基取代基的均烯丙基醇可平稳地转化为β-氯四氢呋喃，产率高达98％。 据报道，通过均烯丙基醇的5-内氯环醚化来构建β-氯四氢呋喃衍生物的有效而温和的方法。该系统在无催化剂的条件下采用磺酰氯作为氯化剂。各种具有芳基或烷基取代基的均烯丙基醇可平稳地转化为β-氯四氢呋喃，产率高达98％。
• Copper-Catalyzed Diastereoselective Synthesis of Trifluoromethylated Tetrahydrofurans
  作者：Yanan Wang、Min Jiang、Jin-Tao Liu

  DOI：10.1002/adsc.201501166

  日期：2016.4.14

  The copper‐catalyzed intramolecular diastereoselective trifluoromethylcycloetherification of homoallylic alcohols with Togni’s reagent as trifluoromethylating reagent was realized under mild conditions. Various trifluoromethylated tetrahydrofurans were synthesized in moderate to good yields. Moreover, a wide range of common functional groups was tolerated.

  在温和的条件下，使用Togni试剂作为三氟甲基化试剂，实现了铜催化的均丙醇的分子内非对映选择性三氟甲基环醚化。以中等至良好的产率合成了各种三氟甲基化的四氢呋喃。而且，宽泛的通用官能团是可以容忍的。
• Regioselective, Asymmetric Formal Hydroamination of Unactivated Internal Alkenes
  作者：Yumeng Xi、Trevor W. Butcher、Jing Zhang、John F. Hartwig

  DOI：10.1002/anie.201509235

  日期：2016.1.11

  We report the regioselective and enantioselective formal hydroamination of unsymmetrical internal alkenes catalyzed by a copper catalyst ligated by DTBM‐SEGPHOS. The regioselectivity of the reaction is controlled by the electronic effects of ether, ester, and sulfonamide groups in the homoallylic position. The observed selectivity underscores the influence of inductive effects of remote substituents

  我们报告了由DTBM-SEGPHOS连接的铜催化剂催化的不对称内部烯烃的区域选择性和对映体选择性加氢胺化反应。反应的区域选择性由在均烯丙基位置的醚，酯和磺酰胺基团的电子效应控制。观察到的选择性强调了远程取代基的感应作用对在烃基上发生的催化过程的选择性的影响，该方法可直接获得各种具有高对映选择性的1,3-氨基醇衍生物。
• Copper-Catalyzed Phosphonation–Annulation Approaches to the Synthesis of β-Phosphonotetrahydrofurans Involving C–P and C–O Bonds Formation
  作者：Yuzhen Gao、Xueqin Li、Weizhu Chen、Guo Tang、Yufen Zhao

  DOI：10.1021/acs.joc.5b02026

  日期：2015.11.20

  Substituted tetrahydrofuran derivatives play important roles as biological activities. A versatile method for the synthesis of beta-phosphonotetrahydrofurans has been developed based on Cu-catalyzed difunctionalization of alkenes. This transformation would provide a new pathway for the formation of Csp(3)-P and Csp(3)-O bonds in one step. Furthermore, this copper catalyst system can be used in the synthesis of beta-phosphonotetrahydropyrans and phosphono-gamma-butyrolactones. These reactions were also performed well by using 3 equiv of Mn(OAc)(3)center dot 2H(2)O as the oxidant without copper catalyst.
• [2,3]-Wittig rearrangement by a chlorine–lithium exchange
  作者：Beatriz Maciá、Cecilia Gómez、Miguel Yus

  DOI：10.1016/j.tetlet.2005.06.160

  日期：2005.9

  reaction of different allylic chloromethyl ethers 1 with an excess of lithium powder (1:7 molar ratio) and a catalytic amount of DTBB (2.5 mol %) in THF at 0 °C for 1 h gives, after hydrolysis with water, the expected alcohols 2 resulting from a [2,3]-Wittig rearrangement, in an exclusive manner. The same process can also be applied to the corresponding [1,2]-Wittig rearrangement, as it is exemplified

  不同的烯丙基氯甲基醚1与过量的锂粉（摩尔比为1：7）和催化量的DTBB（2.5 mol％）在THF中的反应在0°C下反应1 h，在用水水解后，得到预期的[2,3] -Wittig重排产生的唯一醇2。如对苄基氯甲基醚所举例说明的，相同的方法也可用于相应的[1,2]-维蒂希重排。