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1-(benzylamino)-1-oxoundecan-4-yl acetate | 1233882-47-7

中文名称
——
中文别名
——
英文名称
1-(benzylamino)-1-oxoundecan-4-yl acetate
英文别名
——
1-(benzylamino)-1-oxoundecan-4-yl acetate化学式
CAS
1233882-47-7
化学式
C20H31NO3
mdl
——
分子量
333.471
InChiKey
BWMNDQFWWPKFOQ-UHFFFAOYSA-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):
    4.38
  • 重原子数:
    24.0
  • 可旋转键数:
    12.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    55.4
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-(benzylamino)-1-oxoundecan-4-yl acetate甲醇 、 Novozym 435 作用下, 以 异丙醚 为溶剂, 反应 24.0h, 以51%的产率得到(R)-1-(benzylamino)-1-oxoundecan-4-yl acetate
    参考文献:
    名称:
    Combination of Novozym 435–Catalyzed Hydrolysis and Mitsunobu Reaction for Production of (R)-γ-Lactones
    摘要:
    Chiral -lactones of both enantiomers were synthesized with more than 90% optical purities. The key step was Novozym 435-catalyzed hydrolysis of racemic N-benzyl-4-acetoxyalkylamides. Additionally, because (R)--lactones are predominant in apricot, mango, peach, passion fruit, and strawberry, synthesis was attempted using only one enantiomer selectively. The (R)-enantimer was synthesized with more than 80% total yield and more than 90% optical purity by a combination of Novozym 435-catalyzed hydrolysis and the Mitsunobu reaction.
    DOI:
    10.1080/00397910903134618
  • 作为产物:
    描述:
    参考文献:
    名称:
    Combination of Novozym 435–Catalyzed Hydrolysis and Mitsunobu Reaction for Production of (R)-γ-Lactones
    摘要:
    Chiral -lactones of both enantiomers were synthesized with more than 90% optical purities. The key step was Novozym 435-catalyzed hydrolysis of racemic N-benzyl-4-acetoxyalkylamides. Additionally, because (R)--lactones are predominant in apricot, mango, peach, passion fruit, and strawberry, synthesis was attempted using only one enantiomer selectively. The (R)-enantimer was synthesized with more than 80% total yield and more than 90% optical purity by a combination of Novozym 435-catalyzed hydrolysis and the Mitsunobu reaction.
    DOI:
    10.1080/00397910903134618
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