3-Azabicyclo[3.3.1]non-6-ene, 1,5-dinitro-3-(phenylmethyl)- | 268216-99-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 3-Azabicyclo[3.3.1]non-6-ene, 1,5-dinitro-3-(phenylmethyl)-
• 英文别名: 3-benzyl-1,5-dinitro-3-azabicyclo[3.3.1]non-6-ene
• CAS: 268216-99-5
• 化学式: C₁₅H₁₇N₃O₄
• 分子量: 303.318
• InChiKey: SRDQDMVAKXLEIV-UHFFFAOYSA-N

物化性质

• 沸点：
  453.0±45.0 °C(Predicted)
• 密度：
  1.34±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  94.9
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-Azabicyclo[3.3.1]non-6-ene, 1,5-dinitro-3-(phenylmethyl)- 在 镍 氢气 、 盐酸 作用下， 以 甲醇 为溶剂， 以70%的产率得到3-benzyl-3-azabicyclo[3.3.1]nonane-1,5-biamine trihydrochloride
  参考文献：
  名称：

  3-氮杂双环[3.3.1]壬烷衍生物：IX。溶液和固态3-氮杂双环[3.3.1]壬烷-1,5-二胺的合成及分子结构

  摘要：

  During catalytic reduction with hydrogen on nickel of a series of 3-substituted 1,5-dinitro-3-azabicyclo-[3.3. 1]non-6-enes alongside nitro groups reduction occurred also hydrogenation of the double bond. New diamines of the 3)-azabicyclo[3.3. I]nonane series were synthesized, and their structure was established by means of IR, H-1 and C-13 NMR spectroscopy and X-ray diffraction study.

  DOI：

  10.1023/b:rujo.0000034950.28394.e0
• 作为产物：
  描述：

  1,3-二硝基苯 、 聚合甲醛 、 苄胺 在 钾硼氢 作用下， 以 四氢呋喃 、 水 为溶剂， 以50%的产率得到3-Azabicyclo[3.3.1]non-6-ene, 1,5-dinitro-3-(phenylmethyl)-
  参考文献：
  名称：

  Atroshchenko; Nikiforova; Gitis, Russian Journal of Organic Chemistry, 1999, vol. 35, # 9, p. 1308 - 1312

  摘要：

  DOI：

文献信息

• Chlorination features of 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes
  作者：Yu. M. Atroshchenko、N. K. Melekhina、I. V. Shakhkel’dyan、I. E. Yakunina、A. N. Shchukin、E. V. Shuvalova、V. A. Subbotin

  DOI：10.1134/s1070428006080203

  日期：2006.8

  The electrophilic chlorine addition to 3-substituted 1,5-dinitro-3-azabicyclo[3.3.1]-non-6-enes in the tetrachloromethane is accompanied at an intramolecular 3,7-cyclization giving 6-chloro-3-R-1,5-dinitro-3-azoniatricyclo[3.3.1.03,7]nonane chlorides. The reaction of the tricyclic quaternary ammonium salts with sodium methoxide leads to the formation of dealkylated and dehydrohalogenated products, 3-substituted 8-chloro-1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes, bicyclic products with a halogen atom in an allyl position with respect to the double bond.
• Atroshchenko; Nikiforova; Gitis, Russian Journal of Organic Chemistry, 1999, vol. 35, # 9, p. 1308 - 1312
  作者：Atroshchenko、Nikiforova、Gitis、Grudtsyn、Shishkin、Andrianov、Shakhkel'dyan

  DOI：——

  日期：——
• 3-Azabicyclo[3.3.1]nonane Derivatives: IX. Synthesis and Molecular Structure of 3-Azabicyclo[3.3.1]nonane-1,5-diamines in Solution and in Solid State
  作者：M. V. Kopyshev、I. V. Shakhkeldyan、L. M. Kozlova、E. F. Litvin、V. Z. Sharf、N. A. Troitskii、Yu. M. Atroshchenko、E. N. Alifanova、M. B. Nikishina、I. N. Vorontsov、D. V. Gurylev

  DOI：10.1023/b:rujo.0000034950.28394.e0

  日期：2004.2

  During catalytic reduction with hydrogen on nickel of a series of 3-substituted 1,5-dinitro-3-azabicyclo-[3.3. 1]non-6-enes alongside nitro groups reduction occurred also hydrogenation of the double bond. New diamines of the 3)-azabicyclo[3.3. I]nonane series were synthesized, and their structure was established by means of IR, H-1 and C-13 NMR spectroscopy and X-ray diffraction study.