(1S,2R)-3-amino-1-(2-ethoxyphenoxy)-1-phenylpropan-2-ol | 1384288-63-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (1S,2R)-3-amino-1-(2-ethoxyphenoxy)-1-phenylpropan-2-ol
• CAS: 1384288-63-4
• 化学式: C₁₇H₂₁NO₃
• 分子量: 287.359
• InChiKey: NSRLBJFRMMPGOK-PBHICJAKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  21
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  64.7
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (1S,2R)-3-amino-1-(2-ethoxyphenoxy)-1-phenylpropan-2-ol 在 dimethyl sulfide borane 、 potassium tert-butylate 、 碳酸氢钠 作用下， 以 四氢呋喃 、 乙醚 、 水 、 叔丁醇 为溶剂， 反应 1.0h， 生成 (2R,3S)-2-[α-(2-ethoxyphenoxy)phenylmethyl]morpholine
  参考文献：
  名称：

  The synthesis of (R,S)-reboxetine employing a tandem cyclic sulfate rearrangement—opening process

  摘要：

  (R,S)-Reboxetine was synthesized in nine steps and with 43% overall yield starting from trans-cinnamyl alcohol. Following silylation and AD steps, the two hydroxyl groups at C-1 and C-2 were simultaneously activated to the cyclic sulfate. A series of tandem reactions initiated by desilylation transposed the activation to C-3, then to C-1, where nucleophilic displacements took place in succession. During this process, the configuration at C-2 was inverted while that at C-1 was retained through a double inversion. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2012.04.018
• 作为产物：
  描述：

  (E)-1-tert-butyldimethylsilyloxy-3-phenyl-2-propene 在 sodium periodate 、 氯化亚砜 、 甲基磺酰胺 、 ruthenium(III) chloride trihydrate 、 AD-mix α 、 palladium 10% on activated carbon 、 四丁基氟化铵 、 水 、 氢气 、 三乙胺 作用下， 以 四氯化碳 、 二氯甲烷 、 水 、 乙酸乙酯 、 乙腈 、 叔丁醇 为溶剂， 反应 11.17h， 生成 (1S,2R)-3-amino-1-(2-ethoxyphenoxy)-1-phenylpropan-2-ol
  参考文献：
  名称：

  The synthesis of (R,S)-reboxetine employing a tandem cyclic sulfate rearrangement—opening process

  摘要：

  (R,S)-Reboxetine was synthesized in nine steps and with 43% overall yield starting from trans-cinnamyl alcohol. Following silylation and AD steps, the two hydroxyl groups at C-1 and C-2 were simultaneously activated to the cyclic sulfate. A series of tandem reactions initiated by desilylation transposed the activation to C-3, then to C-1, where nucleophilic displacements took place in succession. During this process, the configuration at C-2 was inverted while that at C-1 was retained through a double inversion. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2012.04.018