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N(1),N(3)-bis(4-chlorophenyl)-N(1),N(3)-dimethylmalonamide | 1028331-25-0

中文名称
——
中文别名
——
英文名称
N(1),N(3)-bis(4-chlorophenyl)-N(1),N(3)-dimethylmalonamide
英文别名
N,N'-bis(4-chlorophenyl)-N,N'-dimethylpropanediamide
N(1),N(3)-bis(4-chlorophenyl)-N(1),N(3)-dimethylmalonamide化学式
CAS
1028331-25-0
化学式
C17H16Cl2N2O2
mdl
——
分子量
351.232
InChiKey
SRMYTBSFAVSNQQ-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):
    3.7
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    N(1),N(3)-bis(4-chlorophenyl)-N(1),N(3)-dimethylmalonamide[双(三氟乙酰氧基)碘]苯 作用下, 以 2,2,2-三氟乙醇 为溶剂, 以60%的产率得到5,5'-dichloro-1,1'-dimethyl-3,3'-spirobi[indoline]-2,2'-dione
    参考文献:
    名称:
    Phenyliodine Bis(trifluoroacetate)-Mediated Oxidative C–C Bond Formation: Synthesis of 3-Hydroxy-2-oxindoles and Spirooxindoles from Anilides
    摘要:
    The reaction of phenyliodine bis(trifluoroacetate) (PIFA) with a series of anilides 1 (E = CO2Et) In CF3CH2OH was found to give 3-hydroxy-2-oxindole derivatives 2, while that with various anilides 1' (E = CON(R-4)Ar) afforded the C-2-symmetric or unsymmetric spirooxindoles 3. These processes feature a metal-free oxidative C(sp(2))-C(sp(3)) bond formation, followed by oxidative hydroxylation or spirocyclization.
    DOI:
    10.1021/ol300418h
  • 作为产物:
    描述:
    丙二酸4-氯-N-甲基苯胺N,N'-二环己基碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 以54%的产率得到N(1),N(3)-bis(4-chlorophenyl)-N(1),N(3)-dimethylmalonamide
    参考文献:
    名称:
    Phenyliodine Bis(trifluoroacetate)-Mediated Oxidative C–C Bond Formation: Synthesis of 3-Hydroxy-2-oxindoles and Spirooxindoles from Anilides
    摘要:
    The reaction of phenyliodine bis(trifluoroacetate) (PIFA) with a series of anilides 1 (E = CO2Et) In CF3CH2OH was found to give 3-hydroxy-2-oxindole derivatives 2, while that with various anilides 1' (E = CON(R-4)Ar) afforded the C-2-symmetric or unsymmetric spirooxindoles 3. These processes feature a metal-free oxidative C(sp(2))-C(sp(3)) bond formation, followed by oxidative hydroxylation or spirocyclization.
    DOI:
    10.1021/ol300418h
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文献信息

  • Iron(III) Containing Complex and Condensation Reaction Catalysts, Methods for Preparing the Catalysts, and Compositions Containing the Catalysts
    申请人:Dow Corning Corporation
    公开号:US20140371056A1
    公开(公告)日:2014-12-18
    A composition is capable of curing via condensation reaction. The composition uses a new condensation reaction catalyst. The new condensation reaction catalyst is used to replace conventional tin catalysts. The composition can react to form a gum, gel, rubber, or resin.
  • US9328205B2
    申请人:——
    公开号:US9328205B2
    公开(公告)日:2016-05-03
  • [EN] IRON(III) CONTAINING COMPLEX AND CONDENSATION REACTION CATALYSTS, METHODS FOR PREPARING THE CATALYSTS, AND COMPOSITIONS CONTAINING THE CATALYSTS<br/>[FR] COMPLEXE CONTENANT DU FER(III)ET CATALYSEURS DE RÉACTION DE CONDENSATION, PROCÉDÉS POUR PRÉPARER CES CATALYSEURS ET COMPOSITIONS CONTENANT CES CATALYSEURS
    申请人:DOW CORNING
    公开号:WO2013052585A2
    公开(公告)日:2013-04-11
    A composition is capable of curing via condensation reaction. The composition uses a new condensation reaction catalyst. The new condensation reaction catalyst is used to replace conventional tin catalysts. The composition can react to form a gum, gel, rubber, or resin.
  • Phenyliodine Bis(trifluoroacetate)-Mediated Oxidative C–C Bond Formation: Synthesis of 3-Hydroxy-2-oxindoles and Spirooxindoles from Anilides
    作者:Junwei Wang、Yucheng Yuan、Rui Xiong、Daisy Zhang-Negrerie、Yunfei Du、Kang Zhao
    DOI:10.1021/ol300418h
    日期:2012.5.4
    The reaction of phenyliodine bis(trifluoroacetate) (PIFA) with a series of anilides 1 (E = CO2Et) In CF3CH2OH was found to give 3-hydroxy-2-oxindole derivatives 2, while that with various anilides 1' (E = CON(R-4)Ar) afforded the C-2-symmetric or unsymmetric spirooxindoles 3. These processes feature a metal-free oxidative C(sp(2))-C(sp(3)) bond formation, followed by oxidative hydroxylation or spirocyclization.
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