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5-(4-hydroxy-3,5-di-isopropylphenyl)thianthreniumyl perchlorate | 134189-27-8

中文名称
——
中文别名
——
英文名称
5-(4-hydroxy-3,5-di-isopropylphenyl)thianthreniumyl perchlorate
英文别名
——
5-(4-hydroxy-3,5-di-isopropylphenyl)thianthreniumyl perchlorate化学式
CAS
134189-27-8
化学式
C24H25OS2*ClO4
mdl
——
分子量
493.045
InChiKey
WSWLKFDYMWLUGM-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

SDS

SDS:9cd525f76ace4e00e6e09bd2189cabd2
查看

反应信息

  • 作为产物:
    描述:
    丙泊酚thianthrene cation radical perchlorate乙腈 为溶剂, 以45%的产率得到噻蒽
    参考文献:
    名称:
    Reactions of phenols with thianthrene cation radical
    摘要:
    The phenols 2-R1-6-R2-phenol 1a-g in which R1 = R2 = tert-butyl, methyl, isopropyl, Cl, Br, F, and H reacted with thianthrene cation radical perchlorate (Th.+ClO4-) to give 5-(4-hydroxyaryl)thianthreniumyl perchlorates 2a-g in good yield. o-Allylphenol (1i) behaved similarly. o-tert-Butylphenol (1h) gave both 5-(3-tert-butyl-4-hydroxyphenyl)thianthreniumyl perchlorate (2h) and a quinonoidal perchlorate (3), namely, 5-(3-thianthreniumyl-5-tert-butyl-6-oxo-2,4-cyclohexadien-1-ylidene)-5,5-dihydrothianthrene perchlorate. The 2,6-di-tert-butyl-4-R3-phenols 4a-c, R3 = tert-butyl, methoxy, and methyl, reacted with Th.+ClO4- in nitrile solvents (RCN) to give 2-R-5-R3-7-tert-butylbenzoxazoles 5a-e. The tert-butyl group that was displaced by RCN in forming 5 was converted into t-BuNHCOR (8), tert-butyl alcohol, and isobutene. In contrast, 2-tert-butyl-4,6-dimethylphenol (9) gave, in CH3CN, 4-tert-butyl-2,5,7-trimethylbenzoxazole (11), that is, with migration of the displaced tert-butyl group. The reactions of 4-tert-butylphenol (14) and 2,4-di-tert-butylphenol (17) are also described.
    DOI:
    10.1021/jo00035a031
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