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9-methoxy-1',1',2',2'-tetramethylspiro[7H-benzo[7]annulene-6,3'-cyclopropane]-5-one | 1060767-48-7

中文名称
——
中文别名
——
英文名称
9-methoxy-1',1',2',2'-tetramethylspiro[7H-benzo[7]annulene-6,3'-cyclopropane]-5-one
英文别名
——
9-methoxy-1',1',2',2'-tetramethylspiro[7H-benzo[7]annulene-6,3'-cyclopropane]-5-one化学式
CAS
1060767-48-7
化学式
C18H22O2
mdl
——
分子量
270.371
InChiKey
WDZVCSXVACVLTM-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):
    4.2
  • 重原子数:
    20
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    、 lithium 4-methoxy-1-naphtholate 以 四氢呋喃 为溶剂, 以26%的产率得到9-methoxy-1',1',2',2'-tetramethylspiro[7H-benzo[7]annulene-6,3'-cyclopropane]-5-one
    参考文献:
    名称:
    A novel synthesis of spiro[2.6]nonadienones by the reaction of magnesium cyclopropylidenes with naphtholates and phenolates
    摘要:
    The sulfoxide-magnesium exchange reaction of aryl 1-chlorocyclopropyl sulfoxides with i-PrMgCl in THF at low temperature gave magnesium cyclopropylidenes. Treatment of the magnesium cyclopropylidenes with lithium naphtholates or phenolates resulted in the formation of spiro[2.6]nonadienones in up to 82% yield. The structure of the spiro[2.6]nonadienones was found to be dependent on the structure of the naphtholates and phenolates. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.07.066
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文献信息

  • A novel synthesis of spiro[2.6]nonadienones by the reaction of magnesium cyclopropylidenes with naphtholates and phenolates
    作者:Tsuyoshi Satoh、Shinobu Nagamoto、Masanobu Yajima、Yukie Yamada、Yuki Ohata、Makoto Tadokoro
    DOI:10.1016/j.tetlet.2008.07.066
    日期:2008.9
    The sulfoxide-magnesium exchange reaction of aryl 1-chlorocyclopropyl sulfoxides with i-PrMgCl in THF at low temperature gave magnesium cyclopropylidenes. Treatment of the magnesium cyclopropylidenes with lithium naphtholates or phenolates resulted in the formation of spiro[2.6]nonadienones in up to 82% yield. The structure of the spiro[2.6]nonadienones was found to be dependent on the structure of the naphtholates and phenolates. (c) 2008 Elsevier Ltd. All rights reserved.
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