(4R)-4-[(2S)-5-bromopentan-2-yl]-2,2-dimethyl-1,3-dioxolane | 202122-38-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (4R)-4-[(2S)-5-bromopentan-2-yl]-2,2-dimethyl-1,3-dioxolane
• CAS: 202122-38-1
• 化学式: C₁₀H₁₉BrO₂
• 分子量: 251.164
• InChiKey: VNOIMQRIXJVZEH-IUCAKERBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  13
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (4R)-4-[(2S)-5-bromopentan-2-yl]-2,2-dimethyl-1,3-dioxolane 在 Lindlar's catalyst 咪唑 、 正丁基锂 、 草酰氯 、 氨 、 氢气 、 sodium 、 4-甲基苯磺酸吡啶 、 lithium 、 二甲基亚砜 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 丙醇 、 二氯甲烷 、 环己烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 16.42h， 生成 (Z,3S,10S)-3-[tert-butyl(dimethyl)silyl]oxy-10-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]undec-5-en-2-one
  参考文献：
  名称：

  Synthesis and Characterization of Upper and Lower Rim Functionalized [6]Cavitands

  摘要：

  A [6]cavitand has been selectively derivatized on both the lower and upper rims. On the lower rim, two out of six potential sites were oxidized to produce a 1,4 substituted [6]cavitand bisketone, which was converted to a corresponding diol as well as a bisacetate [6]cavitand. The crystal structures of the bisketone and the diol were solved. On the upper rim, all six ArCH3 groups were selectively brominated to ArCH2Br groups to produce the hexabromomethyl [6]cavitand, which was converted to the corresponding hexabenzylthiol and hexabenzylthioacetate [6]cavitands. The conformational properties of all compounds are discussed.

  DOI：

  10.1002/1521-3765(20020816)8:16<3717::aid-chem3717>3.0.co;2-g
• 作为产物：
  描述：

  (2S,3R)-3,7-dimethyl-2,3-epoxy-6-octen-1-ol 在 吡啶 、 硫酸 、 三氟化硼乙醚 、 sodium cyanoborohydride 、 potassium carbonate 、 臭氧 、 lithium bromide 作用下， 以 四氢呋喃 、 二氯甲烷 、 丙酮 为溶剂， 反应 16.25h， 生成 (4R)-4-[(2S)-5-bromopentan-2-yl]-2,2-dimethyl-1,3-dioxolane
  参考文献：
  名称：

  Synthesis and Characterization of Upper and Lower Rim Functionalized [6]Cavitands

  摘要：

  A [6]cavitand has been selectively derivatized on both the lower and upper rims. On the lower rim, two out of six potential sites were oxidized to produce a 1,4 substituted [6]cavitand bisketone, which was converted to a corresponding diol as well as a bisacetate [6]cavitand. The crystal structures of the bisketone and the diol were solved. On the upper rim, all six ArCH3 groups were selectively brominated to ArCH2Br groups to produce the hexabromomethyl [6]cavitand, which was converted to the corresponding hexabenzylthiol and hexabenzylthioacetate [6]cavitands. The conformational properties of all compounds are discussed.

  DOI：

  10.1002/1521-3765(20020816)8:16<3717::aid-chem3717>3.0.co;2-g

文献信息

• Chiral Synthesis of the C_3-13 Segment of Epothilone A
  作者：Zhi-Yu Liu、Chen-Zhi Yu、Jia-De Yang

  DOI：10.1055/s-1997-1076

  日期：——

  Synthesis of the title compound using inexpensive geraniol as starting material in 13 steps and in 10.6% overall yield is described.

  以廉价的香叶醇为起始原料，通过 13 个步骤合成了标题化合物，总收率为 10.6%。
• Synthesis and Characterization of Upper and Lower Rim Functionalized [6]Cavitands
  作者：Christoph Naumann、Brian O. Patrick、John Sherman

  DOI：10.1002/1521-3765(20020816)8:16<3717::aid-chem3717>3.0.co;2-g

  日期：2002.8.16

  A [6]cavitand has been selectively derivatized on both the lower and upper rims. On the lower rim, two out of six potential sites were oxidized to produce a 1,4 substituted [6]cavitand bisketone, which was converted to a corresponding diol as well as a bisacetate [6]cavitand. The crystal structures of the bisketone and the diol were solved. On the upper rim, all six ArCH3 groups were selectively brominated to ArCH2Br groups to produce the hexabromomethyl [6]cavitand, which was converted to the corresponding hexabenzylthiol and hexabenzylthioacetate [6]cavitands. The conformational properties of all compounds are discussed.