methyl 2-((2-methylhex-5-en-3-yl)oxy)acetate | 1318230-38-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: methyl 2-((2-methylhex-5-en-3-yl)oxy)acetate
• CAS: 1318230-38-4
• 化学式: C₁₀H₁₈O₃
• 分子量: 186.251
• InChiKey: YVBARXIHFJETQL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.78
• 重原子数：
  13.0
• 可旋转键数：
  6.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  35.53
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  methyl 2-((2-methylhex-5-en-3-yl)oxy)acetate 、 溶剂黄146 在 [1,2-bis-(phenylsulfinyl)ethane]palladium(II) acetate 、 (1R,2R)-(-)-[1,2-cyclohexanediamine-N,N'-bis(3,5-di-tert-butylsalicylidine)] chromium(III) chloride 、 对苯醌 作用下， 以 1,4-二氧六环 为溶剂， 反应 72.0h， 以10%的产率得到methyl (E)-2-((6-acetoxy-2-methylhex-4-en-3-yl)oxy)acetate
  参考文献：
  名称：

  Synthetic Versatility in C–H Oxidation: A Rapid Approach to Differentiated Diols and Pyrans from Simple Olefins

  摘要：

  Conventionally, C-H oxidation reactions are used to install functional groups. The use of C-H oxidation to transform simple starting materials into highly versatile intermediates, which enable rapid access to a range of complex target structures, is a new area with tremendous potential in synthesis. Herein we report a Pd(II)/sulfoxide-catalyzed allylic C-H oxidation to form anti-1,4-dioxan-2-ones from homoallylic oxygenates. These versatile building blocks are rapidly elaborated to differentiated syn-1,2-diols, stereo-defined amino-polyols, and syn-pyrans, structures ubiquitous in medicinally important complex molecules found in Nature. We also demonstrate that a C-H oxidation approach to the synthesis of these motifs is orthogonal and complementary to other state-of-the-art methods.

  DOI：

  10.1021/ja206013j
• 作为产物：
  描述：

  (3R)-2-methyl-hex-5-en-3-ol 在 sodium hydride 、 potassium carbonate 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 5.0h， 生成 methyl 2-((2-methylhex-5-en-3-yl)oxy)acetate
  参考文献：
  名称：

  Synthetic Versatility in C–H Oxidation: A Rapid Approach to Differentiated Diols and Pyrans from Simple Olefins

  摘要：

  Conventionally, C-H oxidation reactions are used to install functional groups. The use of C-H oxidation to transform simple starting materials into highly versatile intermediates, which enable rapid access to a range of complex target structures, is a new area with tremendous potential in synthesis. Herein we report a Pd(II)/sulfoxide-catalyzed allylic C-H oxidation to form anti-1,4-dioxan-2-ones from homoallylic oxygenates. These versatile building blocks are rapidly elaborated to differentiated syn-1,2-diols, stereo-defined amino-polyols, and syn-pyrans, structures ubiquitous in medicinally important complex molecules found in Nature. We also demonstrate that a C-H oxidation approach to the synthesis of these motifs is orthogonal and complementary to other state-of-the-art methods.

  DOI：

  10.1021/ja206013j