2,4-di-tert-butyl-6-(3-hydroxy-3-methylbut-1-ynyl)phenol | 936856-58-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2,4-di-tert-butyl-6-(3-hydroxy-3-methylbut-1-ynyl)phenol
• CAS: 936856-58-5
• 化学式: C₁₉H₂₈O₂
• 分子量: 288.43
• InChiKey: SKUOWMMIJAXYLX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.11
• 重原子数：
  21.0
• 可旋转键数：
  0.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.58
• 拓扑面积：
  40.46
• 氢给体数：
  2.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  2,4-di-tert-butyl-6-(3-hydroxy-3-methylbut-1-ynyl)phenol 在 sodium tetrahydroborate 、 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 以96%的产率得到2,4-di-tert-butyl-6-(3-methylbut-1-ynyl)phenol
  参考文献：
  名称：

  Steric buttressing in the Pauson–Khand reactions of aryl enynes

  摘要：

  A variety of aryl enynes have been constructed from o-iodophenol derivatives containing ortho-tert-butyl groups via O-alkylation and a Sonogashira cross-coupling reaction. These substrates undergo efficient thermal and oxidative intramolecular Pauson-Khand reactions leading to the formation of sterically congested cyclopentenones, as well as the formation of medium-sized rings, although in the latter case with unusual regioselectivity. Incorporation of a TMS moiety on the alkyne group in a higher homolog led to cyclization via the normal mode, albeit in relatively low yield. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2007.03.131
• 作为产物：
  描述：

  2,4-二叔丁基苯酚 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide N-碘代丁二酰亚胺 、 三乙胺 作用下， 以 1,4-二氧六环 、 N,N-二甲基甲酰胺 为溶剂， 反应 5.0h， 生成 2,4-di-tert-butyl-6-(3-hydroxy-3-methylbut-1-ynyl)phenol
  参考文献：
  名称：

  Steric buttressing in the Pauson–Khand reactions of aryl enynes

  摘要：

  A variety of aryl enynes have been constructed from o-iodophenol derivatives containing ortho-tert-butyl groups via O-alkylation and a Sonogashira cross-coupling reaction. These substrates undergo efficient thermal and oxidative intramolecular Pauson-Khand reactions leading to the formation of sterically congested cyclopentenones, as well as the formation of medium-sized rings, although in the latter case with unusual regioselectivity. Incorporation of a TMS moiety on the alkyne group in a higher homolog led to cyclization via the normal mode, albeit in relatively low yield. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2007.03.131