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tert-butyl (2S,2'R)-1'-((R)-tert-butylsulfinyl)-2,2'-bipyrrolidine-1-carboxylate | 1224300-77-9

中文名称
——
中文别名
——
英文名称
tert-butyl (2S,2'R)-1'-((R)-tert-butylsulfinyl)-2,2'-bipyrrolidine-1-carboxylate
英文别名
——
tert-butyl (2S,2'R)-1'-((R)-tert-butylsulfinyl)-2,2'-bipyrrolidine-1-carboxylate化学式
CAS
1224300-77-9
化学式
C17H32N2O3S
mdl
——
分子量
344.519
InChiKey
KFEZKFIZZZTKNA-QUVIJQCPSA-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

物化性质

  • 沸点:
    451.2±47.0 °C(Predicted)
  • 密度:
    1.15±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.31
  • 重原子数:
    23.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    49.85
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    tert-butyl (2S,2'R)-1'-((R)-tert-butylsulfinyl)-2,2'-bipyrrolidine-1-carboxylate盐酸 作用下, 以 1,4-二氧六环甲醇 为溶剂, 反应 4.0h, 以88%的产率得到meso-(2S,2'R)-2,2'-bipyrrolidine
    参考文献:
    名称:
    Short asymmetric synthesis of (S,S)-PDP using l-prolinol derivative as economic starting material
    摘要:
    (S,S)-PDP (5d) and its backbone (2S2'S)-bipyrioldine (1) have been extensively applied as the scaffold of various chiral ligands in catalytic asymmetric syntheses In this study, new short asymmetric syntheses of these two important C-2-symmetrical nitrogen heterocycles have been accomplished employing economically available t-prolinol derivative 10 as the starting material Excellent diastereoselectivity was achieved of the key Grignard addition to imine intermediate utilizing (S)-N-tert-butanesulfinamide as the chiral auxiliary (C) 2010 Elsevier Ltd All rights reserved
    DOI:
    10.1016/j.tet.2010.02.048
  • 作为产物:
    描述:
    在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 以3.75 g的产率得到tert-butyl (2S,2'R)-1'-((R)-tert-butylsulfinyl)-2,2'-bipyrrolidine-1-carboxylate
    参考文献:
    名称:
    Short asymmetric synthesis of (S,S)-PDP using l-prolinol derivative as economic starting material
    摘要:
    (S,S)-PDP (5d) and its backbone (2S2'S)-bipyrioldine (1) have been extensively applied as the scaffold of various chiral ligands in catalytic asymmetric syntheses In this study, new short asymmetric syntheses of these two important C-2-symmetrical nitrogen heterocycles have been accomplished employing economically available t-prolinol derivative 10 as the starting material Excellent diastereoselectivity was achieved of the key Grignard addition to imine intermediate utilizing (S)-N-tert-butanesulfinamide as the chiral auxiliary (C) 2010 Elsevier Ltd All rights reserved
    DOI:
    10.1016/j.tet.2010.02.048
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