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1-[5-tert-butyl-2-(4-methoxybenzyloxy)-phenyl]-2-methoxymethoxyethanone | 726180-47-8

中文名称
——
中文别名
——
英文名称
1-[5-tert-butyl-2-(4-methoxybenzyloxy)-phenyl]-2-methoxymethoxyethanone
英文别名
1-[5-Tert-butyl-2-[(4-methoxyphenyl)methoxy]phenyl]-2-(methoxymethoxy)ethanone
1-[5-tert-butyl-2-(4-methoxybenzyloxy)-phenyl]-2-methoxymethoxyethanone化学式
CAS
726180-47-8
化学式
C22H28O5
mdl
——
分子量
372.461
InChiKey
QJMUMAVGTAOBOQ-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):
    4.5
  • 重原子数:
    27
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    54
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    1-[5-tert-butyl-2-(4-methoxybenzyloxy)-phenyl]-2-methoxymethoxyethanone盐酸羟胺sodium acetate 作用下, 以 乙醇 为溶剂, 生成 1-[5-tert-Butyl-2-(4-methoxy-benzyloxy)-phenyl]-2-methoxymethoxy-ethanone oxime
    参考文献:
    名称:
    Asymmetric Hydrogenation of o-Alkoxy-Substituted Arylenamides
    摘要:
    A series of (2-alkoxyaryl)glycinols have been prepared in up to 97.8% ee by asymmetric hydrogenation with cationic rhodium Me-BPE or Me-DuPhos complexes. Others have shown that the presence of ortho substituents on related alpha-arylenamides causes a decrease in enantioselectivity. However, in this study it was found that o-alkoxy alpha-arylenamides were reduced with high enantio selectivity irrespective of substituent size.
    DOI:
    10.1021/jo049723h
  • 作为产物:
    描述:
    1-[5-tert-Butyl-2-(4-methoxy-benzyloxy)-phenyl]-ethanone 在 盐酸 、 lithium hydride 、 三乙胺间氯过氧苯甲酸 作用下, 以 乙醚二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 生成 1-[5-tert-butyl-2-(4-methoxybenzyloxy)-phenyl]-2-methoxymethoxyethanone
    参考文献:
    名称:
    Asymmetric Hydrogenation of o-Alkoxy-Substituted Arylenamides
    摘要:
    A series of (2-alkoxyaryl)glycinols have been prepared in up to 97.8% ee by asymmetric hydrogenation with cationic rhodium Me-BPE or Me-DuPhos complexes. Others have shown that the presence of ortho substituents on related alpha-arylenamides causes a decrease in enantioselectivity. However, in this study it was found that o-alkoxy alpha-arylenamides were reduced with high enantio selectivity irrespective of substituent size.
    DOI:
    10.1021/jo049723h
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