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dimethyl 2-(3-chlorophenyl)-1-tosyl-5-(trifluoromethyl)-1H-pyrrole-3,4-dicarboxylate | 1619266-79-3

中文名称
——
中文别名
——
英文名称
dimethyl 2-(3-chlorophenyl)-1-tosyl-5-(trifluoromethyl)-1H-pyrrole-3,4-dicarboxylate
英文别名
Dimethyl 2-(3-chlorophenyl)-1-(4-methylphenyl)sulfonyl-5-(trifluoromethyl)pyrrole-3,4-dicarboxylate;dimethyl 2-(3-chlorophenyl)-1-(4-methylphenyl)sulfonyl-5-(trifluoromethyl)pyrrole-3,4-dicarboxylate
dimethyl 2-(3-chlorophenyl)-1-tosyl-5-(trifluoromethyl)-1H-pyrrole-3,4-dicarboxylate化学式
CAS
1619266-79-3
化学式
C22H17ClF3NO6S
mdl
——
分子量
515.894
InChiKey
NWDXPNZELLOTGF-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):
    5.2
  • 重原子数:
    34
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    100
  • 氢给体数:
    0
  • 氢受体数:
    9

反应信息

  • 作为产物:
    描述:
    三氟乙酸酐 、 (E)-2-[(3-chlorophenyl)(toluene-4-sulfonylimino)methyl]but-2-enedioic acid dimethyl ester 在 三苯基膦 作用下, 以 二氯甲烷 为溶剂, 以95%的产率得到dimethyl 2-(3-chlorophenyl)-1-tosyl-5-(trifluoromethyl)-1H-pyrrole-3,4-dicarboxylate
    参考文献:
    名称:
    Phosphine-mediated synthesis of trifluoromethyl substituted pyrroles using TFAA as the CF3 source
    摘要:
    A phosphine-mediated synthesis of trifluoromethyl substituted pyrrole derivatives was achieved. The method described here is very fast, operationally simple, and easily amenable to scale-up, and commercially available trifluoroacetic anhydride (TFAA) is used as the only trifluoromethyl source. A wide range of products were obtained with good yields under mild condition using this method. 0(C)2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2014.05.127
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文献信息

  • Phosphine-mediated synthesis of trifluoromethyl substituted pyrroles using TFAA as the CF3 source
    作者:Dan-Dan Tang、Yao Wang、Jun-Ru Wang、Peng-Fei Xu
    DOI:10.1016/j.tetlet.2014.05.127
    日期:2014.7
    A phosphine-mediated synthesis of trifluoromethyl substituted pyrrole derivatives was achieved. The method described here is very fast, operationally simple, and easily amenable to scale-up, and commercially available trifluoroacetic anhydride (TFAA) is used as the only trifluoromethyl source. A wide range of products were obtained with good yields under mild condition using this method. 0(C)2014 Elsevier Ltd. All rights reserved.
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