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(1-(2-(benzyloxy)naphthalen-1-yl)naphthalen-2-yl)(phenyl)methanol | 1370021-72-9

中文名称
——
中文别名
——
英文名称
(1-(2-(benzyloxy)naphthalen-1-yl)naphthalen-2-yl)(phenyl)methanol
英文别名
——
(1-(2-(benzyloxy)naphthalen-1-yl)naphthalen-2-yl)(phenyl)methanol化学式
CAS
1370021-72-9
化学式
C34H26O2
mdl
——
分子量
466.579
InChiKey
LIWAIBUHBDKLSO-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

反应信息

  • 作为产物:
    描述:
    1-[2-[Hydroxy(phenyl)methyl]naphthalen-1-yl]naphthalen-2-ol 、 溴甲苯potassium carbonate 作用下, 以 丙酮 为溶剂, 反应 6.5h, 以86%的产率得到(1-(2-(benzyloxy)naphthalen-1-yl)naphthalen-2-yl)(phenyl)methanol
    参考文献:
    名称:
    A Lewis acid-promoted reduction of acylsilanes to α-hydroxysilanes by diethylzinc
    摘要:
    We report here the first example of the reduction of acylsilanes to alpha-hydroxysilanes, in which diethylzinc was used as a highly reactive agent in the presence of Ti(OiPr)(4) or other Lewis acids. The reduction typically proceeds to give synthetically useful alpha-hydroxysilanes in good yields. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.02.059
  • 作为试剂:
    描述:
    参考文献:
    名称:
    A Lewis acid-promoted reduction of acylsilanes to α-hydroxysilanes by diethylzinc
    摘要:
    We report here the first example of the reduction of acylsilanes to alpha-hydroxysilanes, in which diethylzinc was used as a highly reactive agent in the presence of Ti(OiPr)(4) or other Lewis acids. The reduction typically proceeds to give synthetically useful alpha-hydroxysilanes in good yields. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.02.059
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