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2-hydroxy-12-(ethyl)-9,9-dimethyl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-one | 1322065-61-1

中文名称
——
中文别名
——
英文名称
2-hydroxy-12-(ethyl)-9,9-dimethyl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-one
英文别名
12-ethyl-2-hydroxy-9,9-dimethyl-10,12-dihydro-8H-benzo[a]xanthen-11-one
2-hydroxy-12-(ethyl)-9,9-dimethyl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-one化学式
CAS
1322065-61-1
化学式
C21H22O3
mdl
——
分子量
322.404
InChiKey
JFQFUFKZBUQSKS-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):
    4.7
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2,7-二羟基萘5,5-二甲基-1,3-环己二酮丙醛氯化铵 作用下, 反应 0.25h, 以88%的产率得到2-hydroxy-12-(ethyl)-9,9-dimethyl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-one
    参考文献:
    名称:
    Ammonium Chloride–Catalyzed One-Pot Synthesis of Tetrahydrobenzo[α]xanthen-11-one Derivatives Under Solvent-Free Conditions
    摘要:
    A one-pot, multicomponent reaction of aldehydes, dimedone, and beta-naphthols is described for the preparation of 12-aryl- or 12-alkyl-8,9,10,12-tetrahydrobenzo[alpha]xanthen-11-one derivatives using ammonium chloride as a mild, inexpensive, and environmentally benign catalyst under solvent-free conditions. Different types of aldehyde and beta-naphthol derivatives are used in the reaction, and in all cases the products were synthesized successfully.
    DOI:
    10.1080/00397911.2010.515340
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文献信息

  • Ammonium Chloride–Catalyzed One-Pot Synthesis of Tetrahydrobenzo[α]xanthen-11-one Derivatives Under Solvent-Free Conditions
    作者:Naser Foroughifar、Akbar Mobinikhaledi、Hassan Moghanian、Reza Mozafari、Hamid R. M. Esfahani
    DOI:10.1080/00397911.2010.515340
    日期:2011.9.15
    A one-pot, multicomponent reaction of aldehydes, dimedone, and beta-naphthols is described for the preparation of 12-aryl- or 12-alkyl-8,9,10,12-tetrahydrobenzo[alpha]xanthen-11-one derivatives using ammonium chloride as a mild, inexpensive, and environmentally benign catalyst under solvent-free conditions. Different types of aldehyde and beta-naphthol derivatives are used in the reaction, and in all cases the products were synthesized successfully.
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