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dimethyl 7-chlorobenzo[b]thiophene-2,3-dicarboxylate | 1429655-23-1

中文名称
——
中文别名
——
英文名称
dimethyl 7-chlorobenzo[b]thiophene-2,3-dicarboxylate
英文别名
Dimethyl 7-chloro-1-benzothiophene-2,3-dicarboxylate;dimethyl 7-chloro-1-benzothiophene-2,3-dicarboxylate
dimethyl 7-chlorobenzo[b]thiophene-2,3-dicarboxylate化学式
CAS
1429655-23-1
化学式
C12H9ClO4S
mdl
——
分子量
284.72
InChiKey
IIAPONPSEKHNQI-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):
    3.6
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    80.8
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    邻氯苯硫酚丁炔二酸二甲酯 在 air 作用下, 以 1,4-二氧六环 为溶剂, 以66%的产率得到dimethyl 7-chlorobenzo[b]thiophene-2,3-dicarboxylate
    参考文献:
    名称:
    Air promoted annulation of thiophenols with alkynes leading to benzothiophenes
    摘要:
    空气促进了硫酚与炔烃的分子间环化反应,形成复杂的苯并噻吩化合物。
    DOI:
    10.1039/c8ob00010g
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文献信息

  • Visible-light-induced synthesis of benzothiophenes and benzoselenophenes via the annulation of thiophenols or 1,2-diphenyldiselane with alkynes
    作者:Xiao-Feng Xia、Guo-Wei Zhang、Su-Li Zhu
    DOI:10.1016/j.tet.2017.03.053
    日期:2017.5
    An effective metal-free photoredox-mediated tandem addition/cyclization reaction of thiophenols or 1,2-diphenyldiselane with alkynes leads to 2,3-disubstituted benzothiophenes and benzoselenophenes. Blue light irradiation of the organic dye, Mes-Acr-Me+, initiates the photoredox catalysis. A series of functional groups could be tolerated under ambient conditions, and good to excellent yields were generated. (C) 2017 Elsevier Ltd. All rights reserved.
  • Direct Benzothiophene Formation via Oxygen-Triggered Intermolecular Cyclization of Thiophenols and Alkynes Assisted by Manganese/PhCOOH
    作者:Kaisheng Liu、Fan Jia、Hui Xi、Yuanming Li、Xiaojian Zheng、Qiaoxia Guo、Baojian Shen、Zhiping Li
    DOI:10.1021/ol400719d
    日期:2013.4.19
    An intermolecular oxidative cyclization between thiophenols and alkynes for benzothiophene formation has been established. A variety of multifunctional benzothiophenes are synthesized. In addition, we demonstrated that the obtained benzothiophenes can be used for further transformation to give diverse benzothiophene derivatives efficiently and selectively.
  • Air promoted annulation of thiophenols with alkynes leading to benzothiophenes
    作者:Yajun Wang、Rui Wu、Shijun Zhao、Zhengjun Quan、Yingpeng Su、Congde Huo
    DOI:10.1039/c8ob00010g
    日期:——

    Air promoted intermolecular annulation of thiophenols with alkynes, leading to complex benzothiophenes, is reported.

    空气促进了硫酚与炔烃的分子间环化反应,形成复杂的苯并噻吩化合物。
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