6,7,8,9-tetrahydro-5,9-methanobenzocyclooctene-10(5H)-one | 28173-02-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 四氢化萘
• 英文名称: 6,7,8,9-tetrahydro-5,9-methanobenzocyclooctene-10(5H)-one
• 英文别名: 5.6.7.8.9.10-Hexahydro-5.9-methanobenzocycloocten-10-on；6,7,8,9-tetrahydro-5H-5,9-methano-benzocycloocten-10-one；6,7,8,9-Tetrahydro-5H-5,9-methano-benzocycloocten-10-on；Tricyclo[7.3.1.02,7]trideca-2,4,6-trien-8-one
• CAS: 28173-02-6
• 化学式: C₁₃H₁₄O
• 分子量: 186.254
• InChiKey: QMQDWTNAYRTAPN-UHFFFAOYSA-N

物化性质

• 熔点：
  120-121 °C
• 沸点：
  108-110 °C(Press: 0.2 Torr)
• 密度：
  1.1138 g/cm3(Temp: 19.5 °C)

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  14
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  6,7,8,9-tetrahydro-5,9-methanobenzocyclooctene-10(5H)-one 在 硫酸 、 硝酸 、 二氧化氮 作用下， 生成 2-nitro-6,7,8,9-tetrahydro-5H-5,9-methano-benzocycloocten-10-one
  参考文献：
  名称：

  Adlerova,E.; Protiva,M., Collection of Czechoslovak Chemical Communications, 1967, vol. 32, p. 3177 - 3185

  摘要：

  DOI：
• 作为产物：
  描述：

  (+/-)-cis-3-Phenyl-cyclohexancarbonsaeure 在 PPA 作用下， 生成 6,7,8,9-tetrahydro-5,9-methanobenzocyclooctene-10(5H)-one
  参考文献：
  名称：

  354.多环化合物的合成。第五部分。3-苄基环己醇的环脱水

  摘要：

  DOI：

  10.1039/jr9560001809

文献信息

• Oxidative cyclization of .delta.,.epsilon.- and .epsilon.,.zeta.-unsaturated enol silyl ethers
  作者：Barry B. Snider、Taesoo Kwon

  DOI：10.1021/jo00303a005

  日期：1990.8
• Oxidative cyclization of .delta.,.epsilon.- and .epsilon.,.zeta.-unsaturated enol silyl ethers and unsaturated siloxycyclopropanes
  作者：Barry B. Snider、Taesoo Kwon

  DOI：10.1021/jo00034a038

  日期：1992.4

  Oxidative cyclization of delta,epsilon- and epsilon,zeta-unsaturated enol silyl ethers 4a and 4b with cupric triflate and cuprous oxide or ceric ammonium nitrate and sodium bicarbonate in acetonitrile provides the tricyclic ketones 5a and 5b stereoselectively. These cyclizations proceed by oxidation of 4 to the cation radical 24 followed by cyclization of 24 to cation radical 27. This cation radical undergoes a second cyclization to give cation radical 30, which loses the silyl group, undergoes a second oxidation, and loses a proton to give 5. The stereochemistry of the cycloadduct is controlled by the stereochemistry of the enol ether. The Z-enol methyl ether (Z)-65 leads mainly to 5a while the E-enol methyl ether (E)-65 leads mainly to 6a. The oxidative cyclizations of 7, 13, 21, and 43 are also described. Oxidation of alpha-allyl silyl enol ethers 34a and 34b leads mainly to oxidation without cyclization to give the alpha,beta-unsaturated ketones 36a and 36b. Oxidative cyclizations of alkynyl silyl enol ethers 56 and 60 lead to 15 and 64, respectively. Oxidation of siloxycyclopropane 74 with Cu(BF4)2 generates cation radical 75, which cyclizes to 76, which is oxidized to give 21% of cyclopentane 77. This suggests that cation radicals are intermediates in the oxidative dimerization of siloxycyclopropanes.
• 15. The dehydration of benzylcyclohexanols
  作者：J. W. Cook、C. L. Hewett

  DOI：10.1039/jr9360000062

  日期：——
• SNIDER, BARRY B.;KWON, TAESOO, J. ORG. CHEM., 55,(1990) N6, C. 4786-4788
  作者：SNIDER, BARRY B.、KWON, TAESOO

  DOI：——

  日期：——