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tert-butyl (3S,4S)-3-ethoxy-4-hydroxy-4-phenylpiperidine-1-carboxylate | 1278402-44-0

中文名称
——
中文别名
——
英文名称
tert-butyl (3S,4S)-3-ethoxy-4-hydroxy-4-phenylpiperidine-1-carboxylate
英文别名
——
tert-butyl (3S,4S)-3-ethoxy-4-hydroxy-4-phenylpiperidine-1-carboxylate化学式
CAS
1278402-44-0
化学式
C18H27NO4
mdl
——
分子量
321.417
InChiKey
QTQFLUAKBKGPFP-YJBOKZPZSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    23
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.61
  • 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)-3-ethoxy-4-hydroxy-4-phenylpiperidine-1-carboxylate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-ethoxy-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:
    碘乙烷4-苯基-3,6-二氢-2H-吡啶-1-羧酸叔丁酯四丁基硫酸氢铵 、 sodium hydroxide 作用下, 以 甲苯 为溶剂, 反应 16.0h, 以92%的产率得到tert-butyl (3S,4S)-3-ethoxy-4-hydroxy-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
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文献信息

  • A highly selective monoalkylation of tert-butyl 3,4-dihydroxy-4-phenylpiperidine-1-carboxylate under phase transfer conditions
    作者:Mark I. Lansdell、David Fradet
    DOI:10.1016/j.tetlet.2011.01.029
    日期:2011.3
    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.
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