trans-5-tridecene | 23051-84-5

• 分子结构分类: 有机化合物 - 碳氢化合物 - 不饱和烃
• 英文名称: trans-5-tridecene
• 英文别名: 5-Tridecene；(E)-5-tridecene；trans-5-Tridecen；trans-Tridecen-(5)；tridec-5t-ene；trans-5-n-Tridecen；trans-n-Tridecen-5；(E)-tridec-5-ene
• CAS: 23051-84-5
• 化学式: C₁₃H₂₆
• 分子量: 182.349
• InChiKey: VDFGUEPMNNLWOZ-PKNBQFBNSA-N

物化性质

• 沸点：
  232.3±7.0 °C(Predicted)
• 密度：
  0.770±0.06 g/cm3(Predicted)
• 保留指数：
  1286;1280

计算性质

• 辛醇/水分配系数(LogP)：
  6.3
• 重原子数：
  13
• 可旋转键数：
  9
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.85
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为产物：
  描述：

  1,5-Tridecadiene 在 5cCVD-A 氢气 作用下， 以 正己烷 为溶剂， 以65.2%的产率得到trans-5-tridecene
  参考文献：
  名称：

  Regioselective Hydrogenation Using Platinum-Support Zeolite Modified by CVD-Method

  摘要：

  通过四乙氧基硅烷的化学气相沉积（CVD）制备了一种铂支持的沸石并在其上覆盖了一层二氧化硅，并对其进行了表面催化特性分析。使用该催化剂系统，证明了在多种不饱和烃的情况下，末端碳-碳双键优先被氢化。此外，还阐明了在该催化剂系统下，对具有多个双键的化合物实现了高度区域选择性氢化。因此，提出了一个关于这一催化剂系统的反应模型。

  DOI：

  10.1246/bcsj.64.2508

文献信息

• 1-Methyl-1H-tetrazol-5-yl (MT) sulfones in the Julia-Kocienski olefination: Comparison with the PT and the TBT sulfones
  作者：Kaori Ando、Daiki Kawano、Daiki Takama、Yutaka Semii

  DOI：10.1016/j.tetlet.2019.05.007

  日期：2019.6

  n-pentyl 1-methyl-1H-tetrazol-5-yl (MT) sulfone 1a in the Julia-Kocienski reactions were compared with those of the PT sulfone 1b and the TBT sulfone 1c. The improved stability of the anion derived from the n-pentyl MT sulfone 1a enhanced the efficiency of the olefination reactions and gave higher yields of the product alkenes 3 compared with the PT sulfone 1b. Especially high E-selectivity and high

  比较了新制备的正戊基1-甲基-1 H-四唑-5-基（MT）砜1a在Julia-Kocienski反应中的稳定性和立体选择性，与PT砜1b和TBT砜1c的稳定性和立体选择性进行了比较。与PT砜1b相比，由正戊基MT砜1a衍生的阴离子的稳定性提高，提高了烯化反应的效率，并提高了烯烃3的产率。从与芳族醛和α，β-不饱和醛的反应中获得特别高的E-选择性和高产率。的选择性与PT砜1b相比，1a对碱抗衡离子的变化不太敏感。具有乙基或更长烷基链的MT砜的反应也以高收率选择性地产生了E-烯烃。
• Stabilization of long-chain intermediates in solution. Octyl radicals and cations
  作者：Aleksandar V. Teodorović、Dalibor M. Badjuk、Nenad Stevanović、Radoslav Z. Pavlović

  DOI：10.1016/j.molstruc.2013.02.020

  日期：2013.5

  The rearrangements of 1-octyl, 1-decyl and 1-tridecyl intermediates obtained from thermal lead(IV) acetate (LTA) decarboxylation of nonanoic, undecanoic and tetradecanoic acid were investigated experimentally through analysis and distribution of the products. The relationships between 1,5-, 1,6- and possibly existing 1,7-homolytic hydrogen transfer in 1-octyl-radical, as well as successive 1,2-hydride shift in corresponding cation have been computed via Monte-Carlo method. Taking into account that ratios of 1,5-/1,6-homolytic rearrangements in 1-octyl- and 1-tridecyl radical are approximately the same, the simulation shows very low involvement of 1,7-hydrogen rearrangement (1,5-/1,6-/1,7-hydrogen rearrangement = 85:31:1) in 1-octyl radical. (C) 2013 Elsevier B.V. All rights reserved.
• Carbon-carbon bond formation by selective coupling of n-alkylcopper reagents with organic halides
  作者：Elias J. Corey、Gary H. Posner

  DOI：10.1021/ja01022a058

  日期：1968.9
• Regioselective Hydrogenation Using Platinum-Support Zeolite Modified by CVD-Method
  作者：Hideyuki Kuno、Makoto Shibagaki、Kyoko Takahashi、Ichiro Honda、Hajime Matsushita

  DOI：10.1246/bcsj.64.2508

  日期：1991.8

  A platinum-support zeolite coupled with a silica layer was prepared by Chemical Vapor Deposition (CVD) of tetraethoxysilane, and was investigated in order to determine the catalytic characterization in an analysis of the surface. With this catalyst system, it was demonstrated that the terminal carbon–carbon double bond is preferentially hydrogenated in the case of several unsaturated hydrocarbons. Further, it was elucidated that a highly regioselective hydrogenation of compounds which possess plural double bonds was achieved over this catalyst system. As a result, a reaction model regarding this catalyst system has been put forward.

  通过四乙氧基硅烷的化学气相沉积（CVD）制备了一种铂支持的沸石并在其上覆盖了一层二氧化硅，并对其进行了表面催化特性分析。使用该催化剂系统，证明了在多种不饱和烃的情况下，末端碳-碳双键优先被氢化。此外，还阐明了在该催化剂系统下，对具有多个双键的化合物实现了高度区域选择性氢化。因此，提出了一个关于这一催化剂系统的反应模型。

表征谱图