(-)-(4S)-4-(tert-butyldimethylsilyl)oxy-5,5-dimethyl-2,6-octanedione | 681029-63-0

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: (-)-(4S)-4-(tert-butyldimethylsilyl)oxy-5,5-dimethyl-2,6-octanedione
• 英文别名: (4S)-4-[tert-butyl(dimethyl)silyl]oxy-5,5-dimethyloctane-2,6-dione
• CAS: 681029-63-0
• 化学式: C₁₆H₃₂O₃Si
• 分子量: 300.514
• InChiKey: HYZVGSJRTIYDME-AWEZNQCLSA-N

物化性质

• 沸点：
  352.8±37.0 °C(Predicted)
• 密度：
  0.912±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.36
• 重原子数：
  20
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  43.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (-)-(4S)-4-(tert-butyldimethylsilyl)oxy-5,5-dimethyl-2,6-octanedione 在 sodium hydroxide 作用下， 以 乙醇 、 水 为溶剂， 反应 1.0h， 以50%的产率得到(+)-(5S)-2,3,6,6-tetramethyl-5-(tert-butyldimethylsilyl)oxycyclohex-2-enone
  参考文献：
  名称：

  Asymmetric aldol reactions using catalytic d(+)-proline: a new, economic and practical approach to a commonly employed C1–C6 keto-acid synthon of the epothilones

  摘要：

  A new approach to ketoacid 4, a common C1-C6 fragment used in the total synthesis of epothilones was initiated by direct aldol reaction of acetone with a pivaldehyde-like substance 5, catalyzed with D-proline, leading to a 2,6-diketoalcohol with better than 99% ee. Further intramolecular closure of the diketone 8 followed by oxidation of the silyl protected hydroxycyclohexenone 14 led to the desired product 4. None of the steps have been optimized, yet the overall yield for the four-step process is 31%. The use of commercially available D-proline to construct the chiral center of 4 under very mild reaction conditions provided an economical and practical method for its construction. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2003.12.048
• 作为产物：
  描述：

  2,2-二甲基-3-氧代戊醛 在 N,N-二异丙基乙胺 、 D-脯氨酸 作用下， 以 二氯甲烷 、 二甲基亚砜 为溶剂， 反应 26.5h， 生成 (-)-(4S)-4-(tert-butyldimethylsilyl)oxy-5,5-dimethyl-2,6-octanedione
  参考文献：
  名称：

  Asymmetric aldol reactions using catalytic d(+)-proline: a new, economic and practical approach to a commonly employed C1–C6 keto-acid synthon of the epothilones

  摘要：

  A new approach to ketoacid 4, a common C1-C6 fragment used in the total synthesis of epothilones was initiated by direct aldol reaction of acetone with a pivaldehyde-like substance 5, catalyzed with D-proline, leading to a 2,6-diketoalcohol with better than 99% ee. Further intramolecular closure of the diketone 8 followed by oxidation of the silyl protected hydroxycyclohexenone 14 led to the desired product 4. None of the steps have been optimized, yet the overall yield for the four-step process is 31%. The use of commercially available D-proline to construct the chiral center of 4 under very mild reaction conditions provided an economical and practical method for its construction. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2003.12.048

文献信息

• Asymmetric aldol reactions using catalytic d(+)-proline: a new, economic and practical approach to a commonly employed C1–C6 keto-acid synthon of the epothilones
  作者：Yansong Zheng、Mitchell A Avery

  DOI：10.1016/j.tet.2003.12.048

  日期：2004.2

  A new approach to ketoacid 4, a common C1-C6 fragment used in the total synthesis of epothilones was initiated by direct aldol reaction of acetone with a pivaldehyde-like substance 5, catalyzed with D-proline, leading to a 2,6-diketoalcohol with better than 99% ee. Further intramolecular closure of the diketone 8 followed by oxidation of the silyl protected hydroxycyclohexenone 14 led to the desired product 4. None of the steps have been optimized, yet the overall yield for the four-step process is 31%. The use of commercially available D-proline to construct the chiral center of 4 under very mild reaction conditions provided an economical and practical method for its construction. (C) 2004 Elsevier Ltd. All rights reserved.