1-(5-methylthiophen-2-yl)butan-1-ol | 879981-00-7

• 分子结构分类: 有机化合物 - 有机杂环化合物
• 英文名称: 1-(5-methylthiophen-2-yl)butan-1-ol
• 英文别名: 1-(5-Methyl-2-thienyl)-1-butanol
• CAS: 879981-00-7
• 化学式: C₉H₁₄OS
• 分子量: 170.276
• InChiKey: DMFAVXXWCAWDLZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  11
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  48.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(5-methylthiophen-2-yl)butan-1-ol 在 lithium aluminium tetrahydride 、 三氯化铝 作用下， 生成 2-正丁基-5-甲基硫代苯
  参考文献：
  名称：

  Side-chain effects on the fragmentation behaviour of alkylthiophenes

  摘要：

  AbstractThe processes leading to the fragment ions formed from alkylthiophene molecule ions by benzylic cleavage without and with transfer of one hydrogen from the side‐chain to the ring and the influence of additional methyl groups on the relative importance of these two fragmentation reactions were investigated.

  DOI：

  10.1002/oms.1210290807
• 作为产物：
  描述：

  5-甲基-2-噻吩甲醛 、 溴丙烷 在 magnesium 作用下， 生成 1-(5-methylthiophen-2-yl)butan-1-ol
  参考文献：
  名称：

  Side-chain effects on the fragmentation behaviour of alkylthiophenes

  摘要：

  AbstractThe processes leading to the fragment ions formed from alkylthiophene molecule ions by benzylic cleavage without and with transfer of one hydrogen from the side‐chain to the ring and the influence of additional methyl groups on the relative importance of these two fragmentation reactions were investigated.

  DOI：

  10.1002/oms.1210290807

文献信息

• Taming furfuryl cations for the synthesis of privileged structures and novel scaffolds
  作者：Seema Dhiman、S. S. V. Ramasastry

  DOI：10.1039/c3ob40814k

  日期：——

  Furfuryl cations are generated via a highly efficient bismuth-catalyzed reaction of furfuryl alcohols. This systematic study provides insight on the reactivity profile of furfuryl cations towards nucleophilic substitution reactions. Novel C–C, C–N, C–O and C–S bond forming reactions of furfuryl cations have been developed, thus providing access to a diverse array of building blocks for further manipulations.

  糠醇正离子通过一种高效率的铋催化糠醇反应生成。这项系统研究揭示了糠醇正离子在亲核取代反应中的反应活性概况。开发了糠醇正离子的新的C-C、C-N、C-O和C-S键形成反应，从而为更深入的分子操作提供了各种多样化的构建模块。
• A new and highly efficient water-soluble copper complex for the oxidation of secondary 1-heteroaryl alcohols by tert-butyl hydroperoxide
  作者：Josée Boudreau、Mike Doucette、Abdelaziz Nait Ajjou

  DOI：10.1016/j.tetlet.2006.01.061

  日期：2006.3

  The water-soluble copper complex generated in situ from CuCl2 and 2,2′-biquinoline-4,4′-dicarboxylic acid dipotassium salt (BQC), has been revealed as a highly efficient and selective catalyst for the oxidation of secondary 1-heteroaryl alcohols to the corresponding heteroaromatic ketones with aqueous tert-butyl hydroperoxide, under mild conditions. The catalytic system is compatible with different

  由CuCl 2和2,2'-联喹啉-4,4'-二羧酸二钾盐（BQC）原位生成的水溶性铜络合物已被证明是一种高效且选择性的催化剂，可氧化次要1-在温和条件下，用叔丁基过氧化氢水溶液将杂芳基醇转变为相应的杂芳族酮。该催化体系与不同的杂环兼容，例如吡啶，吡咯，吲哚，噻吩，呋喃，噻唑和咪唑。