tert-butyl (3S,4S)-4-hydroxy-3-methoxy-4-phenylpiperidine-1-carboxylate | 1278402-43-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: tert-butyl (3S,4S)-4-hydroxy-3-methoxy-4-phenylpiperidine-1-carboxylate
• CAS: 1278402-43-9
• 化学式: C₁₇H₂₅NO₄
• 分子量: 307.39
• InChiKey: LDLYFRAEHSILPW-YOEHRIQHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  59
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  tert-butyl (3S,4S)-4-hydroxy-3-methoxy-4-phenylpiperidine-1-carboxylate 在 盐酸 作用下， 以 1,4-二氧六环 为溶剂， 以100%的产率得到(3S,4S)-3-methoxy-4-phenylpiperidin-4-ol
  参考文献：
  名称：

  A highly selective monoalkylation of tert-butyl 3,4-dihydroxy-4-phenylpiperidine-1-carboxylate under phase transfer conditions

  摘要：

  Liquid-liquid phase transfer conditions have been found to provide highly selective monoalkylation of tert-butyl 3,4-dihydroxy-4-phenylpiperidine-1-carboxylate, a transformation for which many other common alkylation protocols proved inadequate. The high preference for 3-O-alkylation in the phase transfer alkylation is emphasised by the absence of diether formation even in the presence of a large excess of reagents. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2011.01.029
• 作为产物：
  描述：

  4-苯基-3,6-二氢-2H-吡啶-1-羧酸叔丁酯 、 碘甲烷 在 四丁基硫酸氢铵 、 sodium hydroxide 作用下， 以 水 、 甲苯 为溶剂， 反应 16.0h， 以96%的产率得到tert-butyl (3S,4S)-4-hydroxy-3-methoxy-4-phenylpiperidine-1-carboxylate
  参考文献：
  名称：

  A highly selective monoalkylation of tert-butyl 3,4-dihydroxy-4-phenylpiperidine-1-carboxylate under phase transfer conditions

  摘要：

  Liquid-liquid phase transfer conditions have been found to provide highly selective monoalkylation of tert-butyl 3,4-dihydroxy-4-phenylpiperidine-1-carboxylate, a transformation for which many other common alkylation protocols proved inadequate. The high preference for 3-O-alkylation in the phase transfer alkylation is emphasised by the absence of diether formation even in the presence of a large excess of reagents. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2011.01.029