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(-)-6-isopropyl-2-cyclohexenone | 271248-31-8

中文名称
——
中文别名
——
英文名称
(-)-6-isopropyl-2-cyclohexenone
英文别名
(6S)-6-propan-2-ylcyclohex-2-en-1-one
(-)-6-isopropyl-2-cyclohexenone化学式
CAS
271248-31-8
化学式
C9H14O
mdl
——
分子量
138.21
InChiKey
RDSYFWVRUCJTON-QMMMGPOBSA-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:
    208.5±10.0 °C(Predicted)
  • 密度:
    0.931±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.18
  • 重原子数:
    10.0
  • 可旋转键数:
    1.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    17.07
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    (-)-6-isopropyl-2-cyclohexenone 、 alkaline earth salt of/the/ methylsulfuric acid 以 四氢呋喃 为溶剂, 反应 1.0h, 以79%的产率得到(2S-顺式)-2-(异丙基)-5-甲基环己烷-1-酮
    参考文献:
    名称:
    Kinetic Resolution of cis-3-Alkylcyclohexene Oxide by a Chiral Lithium Amide - An Application to a Synthesis of Both Enantiomers of Isomenthon -
    摘要:
    Kinetic resolution of cis-3-alkylcyclohexene oxide (1) was examined using chiral lithium amide, lithium (S)-2-(pyrrolidin-1-yl)methylpyrrolidide (2). High cc (84-->98% eel of 1 was obtained by using 1.1-1.2 equiv of 2, while 6-alkyl-2-cyclohexenol (3) was obtained in moderate ee (60-68% eel by using 0.5-0.75 equiv of 2. Both enantiomers of cis-2-isopropyl-5-methylcyclohexanone (isomenthone)were derived from (1S,2R,3R)-(+)-3-isopropylcyclohexene oxide (1b) or (1R,6R)-(-)-6-isopropyl-2-cyclohexenol (3b) in a few steps, respectively.
    DOI:
    10.3987/com-99-s122
  • 作为产物:
    描述:
    (1S,6S)-(+)-6-isopropyl-2-cyclohexenolmanganese(IV) oxide 作用下, 以 二氯甲烷 为溶剂, 反应 6.0h, 以88%的产率得到(-)-6-isopropyl-2-cyclohexenone
    参考文献:
    名称:
    Kinetic Resolution of cis-3-Alkylcyclohexene Oxide by a Chiral Lithium Amide - An Application to a Synthesis of Both Enantiomers of Isomenthon -
    摘要:
    Kinetic resolution of cis-3-alkylcyclohexene oxide (1) was examined using chiral lithium amide, lithium (S)-2-(pyrrolidin-1-yl)methylpyrrolidide (2). High cc (84-->98% eel of 1 was obtained by using 1.1-1.2 equiv of 2, while 6-alkyl-2-cyclohexenol (3) was obtained in moderate ee (60-68% eel by using 0.5-0.75 equiv of 2. Both enantiomers of cis-2-isopropyl-5-methylcyclohexanone (isomenthone)were derived from (1S,2R,3R)-(+)-3-isopropylcyclohexene oxide (1b) or (1R,6R)-(-)-6-isopropyl-2-cyclohexenol (3b) in a few steps, respectively.
    DOI:
    10.3987/com-99-s122
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