2-羟基癸烷-4-酮 | 88729-56-0

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 中文名称: 2-羟基癸烷-4-酮
• 英文名称: 2-Hydroxydecan-4-one
• CAS: 88729-56-0
• 化学式: C₁₀H₂₀O₂
• 分子量: 172.268
• InChiKey: HUMGMASIYJVTOM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  12
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  (己基磺酰基)苯 在 正丁基锂 、 aluminium amalgam 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 9.5h， 生成 2-羟基癸烷-4-酮
  参考文献：
  名称：

  Syntheses of hydroxy ketones from lactones

  摘要：

  DOI：

  10.1021/jo00181a022

文献信息

• Efficient Method for the Deprotection of <i>tert</i>-Butyldimethylsilyl Ethers with TiCl₄−Lewis Base Complexes:  Application to the Synthesis of 1β-Methylcarbapenems
  作者：Akira Iida、Hiroki Okazaki、Tomonori Misaki、Makoto Sunagawa、Akira Sasaki、Yoo Tanabe

  DOI：10.1021/jo0604484

  日期：2006.7.1

  TiCl4-Lewis base (AcOEt, CH3NO2) complexes smoothly deprotected tert-butyldimethylsilyl (TBDMS) ethers. The reaction velocity with these complexes, which seemed less reactive due to the influence of Lewis bases, was considerably greater than that with TiCl4 alone. Selective desilylations between aliphatic and aromatic TBDMS ethers (1 and 5), between 1 and benzyl, allyl, tosyl, methoxyphenyl, and chloroacetyl ethers (13, 14, 15, 16, and 17), and between TBDMS and TBDPS ethers (18 and 19) were successfully performed. Desilylation of TBDMS-aldol, acyloin, and beta-lactam analogues 9-12 proceeded smoothly due to anchimeric assistance by the neighboring carbonyl groups. The present method was successfully applied to the practical synthesis of 1 beta-methylcarbapenems 20a'-f'.
• CAVICCHIOLI, S.;SAVOIA, D.;TROMBINI, C.;UMANI-RONCHI, A., J. ORG. CHEM., 1984, 49, N 7, 1246-1251
  作者：CAVICCHIOLI, S.、SAVOIA, D.、TROMBINI, C.、UMANI-RONCHI, A.

  DOI：——

  日期：——
• Syntheses of hydroxy ketones from lactones
  作者：Silvia Cavicchioli、Diego Savoia、Claudio Trombini、Achille Umani-Ronchi

  DOI：10.1021/jo00181a022

  日期：1984.4