(Z)-5-benzyldimethylsilyl-2-hexyl-4-pentenoic acid | 639086-26-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (Z)-5-benzyldimethylsilyl-2-hexyl-4-pentenoic acid
• CAS: 639086-26-3
• 化学式: C₂₀H₃₂O₂Si
• 分子量: 332.558
• InChiKey: LTWIPVCHJYBRJR-WJDWOHSUSA-N

物化性质

• 沸点：
  440.3±38.0 °C(Predicted)
• 密度：
  0.964±0.06 g/cm3(Predicted)

反应信息

• 作为反应物：
  描述：

  (Z)-5-benzyldimethylsilyl-2-hexyl-4-pentenoic acid 在 对甲苯磺酸 作用下， 以 氯仿 为溶剂， 反应 20.0h， 生成 trans-2-benzyldimethylsilylmethyl-4-hexyltetrahydrofuran
  参考文献：
  名称：

  Acid-catalyzed intramolecular addition of a carboxy group to vinylsilanes

  摘要：

  In the presence of a catalytic amount of (TsOHH2O)-H-. or TiCl4, 5-silyl-4-pentenoic acids (1), namely vinylsilanes with a carboxy group, were smoothly cyclized to gamma-lactones in good to high yields. The difference in the geometry of the carbon-carbon double-bond did not affect the reaction rate. The TiCl4-catalyzed cyclization of the substrates bearing a phenyl or alkyl group at the homoallylic position showed moderate cis-selectivity, while introduction of a substituent into the allylic position led to high transselectivity. (C) 2003 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/s0022-328x(03)00533-3
• 作为产物：
  描述：

  2-[(Z)-3-(Benzyl-dimethyl-silanyl)-allyl]-octan-1-ol 在 重铬酸吡啶 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 20.0h， 生成 (Z)-5-benzyldimethylsilyl-2-hexyl-4-pentenoic acid
  参考文献：
  名称：

  Acid-catalyzed intramolecular addition of a carboxy group to vinylsilanes

  摘要：

  In the presence of a catalytic amount of (TsOHH2O)-H-. or TiCl4, 5-silyl-4-pentenoic acids (1), namely vinylsilanes with a carboxy group, were smoothly cyclized to gamma-lactones in good to high yields. The difference in the geometry of the carbon-carbon double-bond did not affect the reaction rate. The TiCl4-catalyzed cyclization of the substrates bearing a phenyl or alkyl group at the homoallylic position showed moderate cis-selectivity, while introduction of a substituent into the allylic position led to high transselectivity. (C) 2003 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/s0022-328x(03)00533-3