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ethyl 3-nitro-1-adamantanecarboxylate

中文名称
——
中文别名
——
英文名称
ethyl 3-nitro-1-adamantanecarboxylate
英文别名
Ethyl 3-nitroadamantane-1-carboxylate
ethyl 3-nitro-1-adamantanecarboxylate化学式
CAS
——
化学式
C13H19NO4
mdl
——
分子量
253.298
InChiKey
LTXTWKLNMULITK-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):
    2.1
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    72.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    金刚烷-1-甲酸乙酯N-羟基邻苯二甲酰亚胺 硝酸 作用下, 以 various solvent(s) 为溶剂, 反应 15.0h, 生成 ethyl 3-nitro-1-adamantanecarboxylate
    参考文献:
    名称:
    N-羟基邻苯二甲酰亚胺催化硝酸硝化烷烃
    摘要:
    在温和条件下使用 N-羟基邻苯二甲酰亚胺 (NHPI) 首次成功实现了烷烃与硝酸的催化硝化反应;发现目前硝化的关键是NHPI与硝酸反应原位生成NO2和邻苯二甲酰亚胺N-氧基自由基。
    DOI:
    10.1039/b102374h
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文献信息

  • PROCESS FOR THE PREPARATION OF NITRO COMPOUNDS AND METHOD FOR THE REMOVAL OF NITROGEN DIOXIDE
    申请人:Daicel Chemical Industries, Ltd.
    公开号:EP1099684A1
    公开(公告)日:2001-05-16
    In the invented process for producing a nitro compound, an organic substrate and nitrogen dioxide are reacted in the presence of oxygen or are reacted in a molar ratio of nitrogen dioxide to the organic substrate of less than 1 to yield a corresponding nitro compound. The reaction may be performed in the presence of N-hydroxyphthalimide or other imide compounds. Such organic substrates include (a) aliphatic hydrocarbons, (b) alicyclic hydrocarbons, (c) non-aromatic heterocyclic compounds each having a carbon atom on a ring, which carbon atom is bonded to a hydrogen atom, (d) compounds each having a carbon-hydrogen bond at the adjacent position to an aromatic ring, and (e) compounds each having a carbon-hydrogen bond at the adjacent position to a carbonyl group. This process can efficiently nitrate an organic substrate even under relatively mild conditions.
    在制备硝基化合物的发明过程中,有机底物和二氧化氮氧气存在下反应,或者在二氧化氮与有机底物的摩尔比小于1的情况下反应,以产生相应的硝基化合物。该反应可以在N-羟基邻苯二甲酰亚胺或其他亚酰胺化合物存在下进行。这样的有机底物包括(a) 脂肪烃,(b) 脂环烃,(c) 非芳香杂环化合物,每个环上的碳原子与氢原子相结合,(d) 每个化合物在芳香环旁边位置具有碳氢键,以及(e) 每个化合物在酮基旁边位置具有碳氢键。这个过程可以在相对温和的条件下有效地对有机底物进行硝化。
  • NITRATION OR CARBOXYLATION CATALYSTS
    申请人:Daicel Chemical Industries, Ltd.
    公开号:EP0897747A1
    公开(公告)日:1999-02-24
    In the presence of an imide compound (e.g., N-hydroxyphthalimide) shown by the following formula (1):    wherein R1 and R2 represent a hydrogen atom, a halogen atom, an alkyl group, an aryl group and a cycloalkyl group, and R1 and R2 may bond together to form a double bond, or an aromatic or non-aromatic ring, and Y is an O or OH, and n denotes 1 to 3; a substrate is allowed to contact with at least one reactant selected from (i) a nitrogen oxide and (ii) a mixture of carbon monoxide and oxygen to be introduced with at least one functional group selected from a nitro group and a carboxyl group. The nitrogen oxide includes, for example, a compound represented by the formula NxOy (e.g., N2O3, NO2). The substrate includes, for example, a compound having a methine carbon atom (e.g., adamantane), a compound having a methyl group or a methylene group at an adjacent moiety of an aromatic ring. According to such reaction, the substrate can be efficiently nitrated or carboxylated even in a mild or moderate condition.
    在存在下式(1)所示的酰亚胺化合物(如 N-羟基邻苯二甲酰亚胺)的情况下: 其中 R1 和 R2 代表氢原子、卤素原子、烷基、芳基和环烷基,R1 和 R2 可键合在一起形成双键或芳香环或非芳香环,Y 是 O 或 OH,n 表示 1 至 3; 让基质与至少一种反应物接触,该反应物选自 (i) 氮氧化物和 (ii) 一氧化碳和氧的混合物,并引入至少一种选自硝基和羧基的官能团。例如,氮氧化物包括由式 NxOy 表示的化合物(如 N2O3NO2)。底物包括例如具有甲基碳原子的化合物(如金刚烷)、在芳香环的相邻分子上具有甲基或亚甲基的化合物。根据这种反应,底物即使在温和或中等条件下也能被有效地硝化或羧化。
  • Adamantane derivative
    申请人:DAICEL CHEMICAL INDUSTRIES, LTD.
    公开号:EP1574494A1
    公开(公告)日:2005-09-14
    In the presence of an imide compound (e.g., N-hydroxyphthalimide) shown by the following formula (1):    wherein R1 and R2 represent a hydrogen atom, a halogen atom, an alkyl group, an aryl group and a cycloalkyl group, and R1 and R2 may bond together to form a double bond, or an aromatic or non-aromatic ring, and Y is an O or OH, and n denotes 1 to 3; a substrate is allowed to contact with at least one reactant selected from (i) a nitrogen oxide and (ii) a mixture of carbon monoxide and oxygen to be introduced with at least one functional group selected from a nitro group and a carboxyl group. The nitrogen oxide includes, for example, a compound represented by the formula NxOy (e.g., N2O3, NO2). The substrate includes, for example, a compound having a methine carbon atom (e.g., adamantane), a compound having a methyl group or a methylene group at an adjacent moiety of an aromatic ring. According to such reaction, the substrate can be efficiently nitrated or carboxylated even in a mild or moderate condition.
    在存在下式(1)所示的酰亚胺化合物(如 N-羟基邻苯二甲酰亚胺)的情况下: 其中 R1 和 R2 代表氢原子、卤素原子、烷基、芳基和环烷基,R1 和 R2 可键合在一起形成双键或芳香环或非芳香环,Y 是 O 或 OH,n 表示 1 至 3; 让基质与至少一种反应物接触,该反应物选自 (i) 氮氧化物和 (ii) 一氧化碳和氧的混合物,并引入至少一种选自硝基和羧基的官能团。例如,氮氧化物包括由式 NxOy 表示的化合物(如 N2O3NO2)。底物包括例如具有甲基碳原子的化合物(如金刚烷)、在芳香环的相邻分子上具有甲基或亚甲基的化合物。根据这种反应,底物即使在温和或中等条件下也能被有效地硝化或羧化。
  • Adamantane derivatives
    申请人:DAICEL CHEMICAL INDUSTRIES, LTD.
    公开号:EP1574495A1
    公开(公告)日:2005-09-14
    An adamantane derivative shown by the following formula (2):
    下式(2)所示的金刚烷生物
  • US6468487B1
    申请人:——
    公开号:US6468487B1
    公开(公告)日:2002-10-22
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