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3-Chloro-2-[(4-methoxyphenyl)methyl]-5-(trifluoromethyl)pyridine

中文名称
——
中文别名
——
英文名称
3-Chloro-2-[(4-methoxyphenyl)methyl]-5-(trifluoromethyl)pyridine
英文别名
——
3-Chloro-2-[(4-methoxyphenyl)methyl]-5-(trifluoromethyl)pyridine化学式
CAS
——
化学式
C14H11ClF3NO
mdl
——
分子量
301.696
InChiKey
VCZBEOFVMCBSAS-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):
    4.3
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    3-氟苯基硼酸3-Chloro-2-[(4-methoxyphenyl)methyl]-5-(trifluoromethyl)pyridine 在 dihydrogen dichloro-bis(di-tert-butylphosphinito-κP)palladium(2-) caesium carbonate 作用下, 以 乙二醇二甲醚 为溶剂, 以94%的产率得到3-(3-Fluorophenyl)-2-[(4-methoxyphenyl)methyl]-5-(trifluoromethyl)pyridine
    参考文献:
    名称:
    Use of highly reactive, versatile and air-stable palladium–phosphinous acid complex [(t-Bu)2P(OH)]2PdCl2 (POPd) as a catalyst for the optimized Suzuki–Miyaura cross-coupling of less reactive heteroaryl chlorides and arylboronic acids
    摘要:
    Using highly reactive air-stable palladium-phosphinous acid complex [(t-Bu)(2)P(OH)](2)PdCl2 (POPd) as a catalyst, synthesis of heteroaryl-aryl cross-coupled products via palladium-catalyzed Suzuki-Miyaura coupling of less reactive substituted 3-chloropyridines with arylboronic acids was achieved in high yields. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.05.010
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文献信息

  • Use of highly reactive, versatile and air-stable palladium–phosphinous acid complex [(t-Bu)2P(OH)]2PdCl2 (POPd) as a catalyst for the optimized Suzuki–Miyaura cross-coupling of less reactive heteroaryl chlorides and arylboronic acids
    作者:Subhash P. Khanapure、David S. Garvey
    DOI:10.1016/j.tetlet.2004.05.010
    日期:2004.6
    Using highly reactive air-stable palladium-phosphinous acid complex [(t-Bu)(2)P(OH)](2)PdCl2 (POPd) as a catalyst, synthesis of heteroaryl-aryl cross-coupled products via palladium-catalyzed Suzuki-Miyaura coupling of less reactive substituted 3-chloropyridines with arylboronic acids was achieved in high yields. (C) 2004 Elsevier Ltd. All rights reserved.
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