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(R)-ethyl 3-(2-methoxyphenylthio)-4,4,4-trifluorobutanoate | 1318254-50-0

中文名称
——
中文别名
——
英文名称
(R)-ethyl 3-(2-methoxyphenylthio)-4,4,4-trifluorobutanoate
英文别名
ethyl (3R)-4,4,4-trifluoro-3-(2-methoxyphenyl)sulfanylbutanoate
(R)-ethyl 3-(2-methoxyphenylthio)-4,4,4-trifluorobutanoate化学式
CAS
1318254-50-0
化学式
C13H15F3O3S
mdl
——
分子量
308.322
InChiKey
KNDPZWGNKBJART-LLVKDONJSA-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):
    3.8
  • 重原子数:
    20
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    60.8
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    2-甲氧基苯硫酚ethyl (Z)-4,4,4-trifluorobut-2-enoate 在 N-((1R,2R)-2-(3-((1R,2R)-2-(dimethylamino)cyclohexyl)thioureido)-1,2-diphenylethyl)-3,5-bis(trifluoromethyl)benzenesulfonamide 作用下, 以 甲苯 为溶剂, 反应 0.5h, 以91%的产率得到(R)-ethyl 3-(2-methoxyphenylthio)-4,4,4-trifluorobutanoate
    参考文献:
    名称:
    Organocatalytic Asymmetric Sulfa-Michael Addition of Thiols to 4,4,4-Trifluorocrotonates
    摘要:
    The first asymmetric sulfa-Michael addition of thiols to 4,4,4-trifluorocrotonates for the construction of a stereogenic center bearing a unique trifluoromethyl group and a sulfur atom has been achieved in high yields and excellent enantioselectivities with a 1 mol % bifunctional organocatalyst. Subsequent transformation led to the expedient preparation of enantioenriched thiochroman-4-one and the key intermediate of the potent inhibitor of MMP-3, (R)-gamma-trifluoromethyl gamma-sulfone hydroxamate.
    DOI:
    10.1021/ol201766k
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文献信息

  • Organocatalytic Asymmetric Sulfa-Michael Addition of Thiols to 4,4,4-Trifluorocrotonates
    作者:Xiu-Qin Dong、Xin Fang、Chun-Jiang Wang
    DOI:10.1021/ol201766k
    日期:2011.8.19
    The first asymmetric sulfa-Michael addition of thiols to 4,4,4-trifluorocrotonates for the construction of a stereogenic center bearing a unique trifluoromethyl group and a sulfur atom has been achieved in high yields and excellent enantioselectivities with a 1 mol % bifunctional organocatalyst. Subsequent transformation led to the expedient preparation of enantioenriched thiochroman-4-one and the key intermediate of the potent inhibitor of MMP-3, (R)-gamma-trifluoromethyl gamma-sulfone hydroxamate.
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