1-Chloro-6-[(oxan-2-yl)oxy]hex-3-yn-2-ol | 651325-30-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氧烷类
• 英文名称: 1-Chloro-6-[(oxan-2-yl)oxy]hex-3-yn-2-ol
• 英文别名: 1-chloro-6-(oxan-2-yloxy)hex-3-yn-2-ol
• CAS: 651325-30-3
• 化学式: C₁₁H₁₇ClO₃
• 分子量: 232.707
• InChiKey: BPWMKKKXWLATAF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  15
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.82
• 拓扑面积：
  38.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-Chloro-6-[(oxan-2-yl)oxy]hex-3-yn-2-ol 在 Lindlar's catalyst 2,6-二甲基吡啶 、 甲醇 、 4-二甲氨基吡啶 、 六氯丙酮 、 四丁基氟化铵 、 氢气 、 sodium hydride 、 对甲苯磺酸 、 三乙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 乙醚 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 13.33h， 生成 (4Z,6E)-2-((Z)-6-Chloro-5-hydroxy-hex-3-enyl)-2,9-bis-methoxycarbonyl-deca-4,6-dienedioic acid dimethyl ester
  参考文献：
  名称：

  Comparative Effects of Conjugated and Deconjugated Isomeric Enones on the Transannular Diels−Alder Reaction

  摘要：

  [GRAPHICS]Two isomeric cyclic trienones 2 and 3 (with four methyl esters at positions 3 and 10) underwent transannular Diels-Alder (TADA) reaction at very different temperatures. This drastic difference could be traced to the capacity of the enone dienophile to be conjugated or unconjugated at the transition state. Molecular modeling could confirm this explanation. The calculated enone proved to be very distorted in transition state ts2, and the TADA reaction temperature was accordingly much higher than the one corresponding to ts3 in which the enone was flat.

  DOI：

  10.1021/ol035791z
• 作为产物：
  描述：

  氯乙醛 、 2-(3-丁炔氧基)四水-2H-吡喃 在 正丁基锂 作用下， 以 四氢呋喃 为溶剂， 反应 0.17h， 以60%的产率得到1-Chloro-6-[(oxan-2-yl)oxy]hex-3-yn-2-ol
  参考文献：
  名称：

  Comparative Effects of Conjugated and Deconjugated Isomeric Enones on the Transannular Diels−Alder Reaction

  摘要：

  [GRAPHICS]Two isomeric cyclic trienones 2 and 3 (with four methyl esters at positions 3 and 10) underwent transannular Diels-Alder (TADA) reaction at very different temperatures. This drastic difference could be traced to the capacity of the enone dienophile to be conjugated or unconjugated at the transition state. Molecular modeling could confirm this explanation. The calculated enone proved to be very distorted in transition state ts2, and the TADA reaction temperature was accordingly much higher than the one corresponding to ts3 in which the enone was flat.

  DOI：

  10.1021/ol035791z

文献信息

• Comparative Effects of Conjugated and Deconjugated Isomeric Enones on the Transannular Diels−Alder Reaction
  作者：Franck Caussanel、Pierre Deslongchamps、Yves L. Dory

  DOI：10.1021/ol035791z

  日期：2003.12.1

  [GRAPHICS]Two isomeric cyclic trienones 2 and 3 (with four methyl esters at positions 3 and 10) underwent transannular Diels-Alder (TADA) reaction at very different temperatures. This drastic difference could be traced to the capacity of the enone dienophile to be conjugated or unconjugated at the transition state. Molecular modeling could confirm this explanation. The calculated enone proved to be very distorted in transition state ts2, and the TADA reaction temperature was accordingly much higher than the one corresponding to ts3 in which the enone was flat.