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(5-乙炔基-2-甲氧基苯基)硼酸 | 884010-40-6

中文名称
(5-乙炔基-2-甲氧基苯基)硼酸
中文别名
——
英文名称
5-ethynyl-2-methoxyphenyl boronic acid
英文别名
(5-Ethynyl-2-methoxyphenyl)boronic acid
(5-乙炔基-2-甲氧基苯基)硼酸化学式
CAS
884010-40-6
化学式
C9H9BO3
mdl
——
分子量
175.98
InChiKey
VHXUTJZLYMQQCD-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):
    -0.64
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    49.7
  • 氢给体数:
    2
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    5-溴-2-甲氧苯基硼酸 在 bis-triphenylphosphine-palladium(II) chloride 甲醇copper(l) iodidepotassium carbonate二乙胺三苯基膦 作用下, 以 N,N-二甲基甲酰胺甲苯 为溶剂, 反应 1.42h, 生成 (5-乙炔基-2-甲氧基苯基)硼酸
    参考文献:
    名称:
    Microwave-assisted synthesis of ethynylarylboronates for the construction of boronic acid-based fluorescent sensors for carbohydrates
    摘要:
    A reliable and operationally simple procedure for the synthesis of 2.2-dimethylpropane-1,3-diyl ethynylaryl boronates 4 was developed. The key step is microwave-facilitated selective formation of 2,2-dimethylpropane-1,3-diyl trimethylsilylethynylaryl boronates by Sonogashira reaction front the corresponding bromides. The use of microwave was found to significantly improve the reaction yield and shorten the reaction time. The 2,2-dimethylpropane-1,3-diyl ethynylaryl boronates 4 prepared can be used in the construction of diboronic acid libraries through [2+3] Huisgen cycloaddition for carbohydrate fluorescent sensor development. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2006.02.012
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文献信息

  • Microwave-assisted synthesis of ethynylarylboronates for the construction of boronic acid-based fluorescent sensors for carbohydrates
    作者:Shi-Long Zheng、Suazette Reid、Na Lin、Binghe Wang
    DOI:10.1016/j.tetlet.2006.02.012
    日期:2006.4
    A reliable and operationally simple procedure for the synthesis of 2.2-dimethylpropane-1,3-diyl ethynylaryl boronates 4 was developed. The key step is microwave-facilitated selective formation of 2,2-dimethylpropane-1,3-diyl trimethylsilylethynylaryl boronates by Sonogashira reaction front the corresponding bromides. The use of microwave was found to significantly improve the reaction yield and shorten the reaction time. The 2,2-dimethylpropane-1,3-diyl ethynylaryl boronates 4 prepared can be used in the construction of diboronic acid libraries through [2+3] Huisgen cycloaddition for carbohydrate fluorescent sensor development. (c) 2006 Elsevier Ltd. All rights reserved.
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