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1-nitroxydiamantane | 941305-71-1

中文名称
——
中文别名
——
英文名称
1-nitroxydiamantane
英文别名
1-Pentacyclo[7.3.1.14,12.02,7.06,11]tetradecanyl nitrate
1-nitroxydiamantane化学式
CAS
941305-71-1
化学式
C14H19NO3
mdl
——
分子量
249.31
InChiKey
VLDVFHVFSQWZOK-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):
    3.7
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    55
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-nitroxydiamantane溶剂黄146尿素 作用下, 以 为溶剂, 生成 diamantan-1-ol
    参考文献:
    名称:
    一锅合成笼型醇
    摘要:
    已经开发出一种有效的一锅法程序,用于合成在桥头位置具有羟基的笼型醇。该程序包括先用硝酸或硝酸与乙酸的混合物进行硝化,然后在尿素存在下进行水解。
    DOI:
    10.1134/s1070428017070028
  • 作为产物:
    描述:
    双金刚烷硝酸 作用下, 以 为溶剂, 生成 1-nitroxydiamantane
    参考文献:
    名称:
    金刚石烃一锅法合成桥头氨基醇
    摘要:
    摘要 已经开发出一种直接从笼形烃合成氨基醇的有效方法。多克可扩展性、良好的产量和一锅法,利用现成的试剂以及合成的便利性,显示了它的实用性。所提出的一锅法包括笼式烃与硝酸的连续反应,中间体硝基衍生物与尿素的进一步胺化,然后在添加浓溶液时将先前产生的胺氧化成氨基醇。H 2 SO 4。
    DOI:
    10.1080/00397911.2023.2177173
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文献信息

  • Synthesis of Diamantane Derivatives in Nitric Acid Media
    作者:Yu. N. Klimochkin、E. A. Ivleva、M. S. Zaborskaya
    DOI:10.1134/s1070428021020081
    日期:2021.2
    Abstract 1-Mono- and 1,4-difunctional diamantane derivatives were synthesized by the reaction of diamantane with nitric acid or a HNO3–AcOH mixture followed by the addition of nitrogen-containing nucleophiles. Methyl N-(diamantan-1-yl)carbamothioate was synthesized from diamantan-1-ol and methyl thiocyanate in sulfuric acid.
    摘要 通过使金刚烷与硝酸或HNO 3 -AcOH混合物反应,然后添加含氮亲核试剂,可以合成1-单-和1,4-双官能金刚烷衍生物。由2-金刚烷-1-醇和硫氰酸甲酯在硫酸中合成了N-(二金刚烷-1-基)氨基甲磺酸甲酯。
  • Method for Producing Substituted Diamantanes
    申请人:Schreiner Peter R.
    公开号:US20100036153A1
    公开(公告)日:2010-02-11
    The invention at hand provides at least dinitroxylated diamantanes. In addition, it provides methods for producing substituted diamantanes with high yields and selectivity. According to the invention, dinitroxylated diamantanes are suitable for being reacted with nucleophiles to form the corresponding disubstituted diamantanes. Surprisingly, it was discovered that at least dinitroxylated or hydroxylated diamantanes are rearranged in the presence of a strong acid, creating at least 4,9-nitroxylated or hydroxylated diamantanes. On the basis of this, 4,9-substituted diamantanes are able to be produced in a targeted manner by reaction with further nucleophiles. Thus, the invention at hand provides the following methods according to the present invention for producing at least disubstituted diamantanes: a) at least dinitroxylation, followed by the substitution of all nitroxy groups by a nucleophile or b) at least dinitroxylation, subsequent rearrangement in the presence of a strong acid, after realised rearrangement all nitroxy groups are replaced by a nucleophile or c) at least dinitroxylation, subsequent reaction with water (as nucleophile), rearrangement of the at least dihydroxylated compound in the presence of a strong acid, after realised rearrangement all hydroxy groups are replaced by another nucleophile.
    该发明提供至少二硝基化二莽烷。此外,它提供了一种高产率和选择性生产取代二莽烷的方法。根据该发明,二硝基化的二莽烷适合与亲核试剂反应,形成相应的二取代二莽烷。令人惊讶的是,在强酸存在的情况下发现,至少二硝基化或羟基化的二莽烷会重排,形成至少4,9-硝基化或羟基化的二莽烷。基于此,通过与进一步的亲核试剂反应,可以有针对性地生产4,9-取代的二莽烷。因此,该发明提供了以下根据本发明的方法,用于生产至少二取代的二莽烷:a) 至少二硝基化,然后用亲核试剂替换所有硝基团或b) 至少二硝基化,后在强酸存在下重排,重排后用亲核试剂替换所有硝基团或c) 至少二硝基化,后与水(作为亲核试剂)反应,在强酸存在下重排,重排后用另一亲核试剂替换所有羟基。
  • One-pot amination of cage hydrocarbons
    作者:M. V. Leonova、M. Yu. Skomorokhov、I. K. Moiseev、Yu. N. Klimochkin
    DOI:10.1134/s1070428015120064
    日期:2015.12
    A one-pot procedure has been proposed for the synthesis of amines directly from cage hydrocarbons. A number of cage amines have been synthesized by treatment of adamantane, its homologs, and structurally related cage hydrocarbons with nitric acid in acetic acid and subsequent addition of urea and heating.
  • US8716539B2
    申请人:——
    公开号:US8716539B2
    公开(公告)日:2014-05-06
  • One-pot synthesis of cage alcohols
    作者:Yu. N. Klimochkin、A. V. Yudashkin、E. O. Zhilkina、E. A. Ivleva、I. K. Moiseev、Ya. F. Oshis
    DOI:10.1134/s1070428017070028
    日期:2017.7
    An efficient one-pot procedure has been developed for the synthesis of cage alcohols with hydroxy groups in the bridgehead positions. The procedure includes initial nitroxylation with nitric acid or a mixture of nitric acid with acetic acid and subsequent hydrolysis in the presence of urea.
    已经开发出一种有效的一锅法程序,用于合成在桥头位置具有羟基的笼型醇。该程序包括先用硝酸或硝酸与乙酸的混合物进行硝化,然后在尿素存在下进行水解。
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