1-Tert-butylsulfanyldecan-2-ol | 152398-26-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-Tert-butylsulfanyldecan-2-ol
• CAS: 152398-26-0
• 化学式: C₁₄H₃₀OS
• 分子量: 246.458
• InChiKey: PWNLHTYSCOAPRF-UHFFFAOYSA-N

物化性质

• 沸点：
  340.6±15.0 °C(Predicted)
• 密度：
  0.907±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  16
• 可旋转键数：
  10
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  45.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-Tert-butylsulfanyldecan-2-ol 在 吡啶 、 4-二甲氨基吡啶 、 sodium hydroxide 、 trimethoxonium tetrafluoroborate 作用下， 以 二氯甲烷 为溶剂， 反应 43.5h， 生成 (R)-1,2-环氧癸烷
  参考文献：
  名称：

  Enzyme assisted synthesis of enantiomerically pure δ-lactones

  摘要：

  Both enantiomeric series of a wide variety of optically pure 6-alkylated delta-lactones - saturated as well as unsaturated - were prepared via an enzyme mediated route. The key reaction step is the nucleophilic ring opening of enantiomerically pure alkyl-oxiranes, accessible via the corresponding beta-hydroxythioethers which can be obtained enantiomerically pure via enzyme catalyzed kinetic resolutions.

  DOI：

  10.1016/s0957-4166(00)80146-9
• 作为产物：
  描述：

  1,2-二甲基丁炔酯 、 叔丁基硫醇 在 sodium hydride 作用下， 生成 1-Tert-butylsulfanyldecan-2-ol
  参考文献：
  名称：

  Enzyme assisted synthesis of enantiomerically pure δ-lactones

  摘要：

  Both enantiomeric series of a wide variety of optically pure 6-alkylated delta-lactones - saturated as well as unsaturated - were prepared via an enzyme mediated route. The key reaction step is the nucleophilic ring opening of enantiomerically pure alkyl-oxiranes, accessible via the corresponding beta-hydroxythioethers which can be obtained enantiomerically pure via enzyme catalyzed kinetic resolutions.

  DOI：

  10.1016/s0957-4166(00)80146-9

文献信息

• TAGUCHI, YOICHI;SUHARA, YASUO, YUKAGAKU, 1982, 31, N 6, 383-387
  作者：TAGUCHI, YOICHI、SUHARA, YASUO

  DOI：——

  日期：——
• Enzyme assisted synthesis of enantiomerically pure δ-lactones
  作者：Bernhard Haase、Manfred P. Schneider

  DOI：10.1016/s0957-4166(00)80146-9

  日期：1993.5

  Both enantiomeric series of a wide variety of optically pure 6-alkylated delta-lactones - saturated as well as unsaturated - were prepared via an enzyme mediated route. The key reaction step is the nucleophilic ring opening of enantiomerically pure alkyl-oxiranes, accessible via the corresponding beta-hydroxythioethers which can be obtained enantiomerically pure via enzyme catalyzed kinetic resolutions.