3-(4-tert-butyl-1-cyclohexenyl)iodobenzene | 163394-75-0

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 3-(4-tert-butyl-1-cyclohexenyl)iodobenzene
• 英文别名: Benzene, 1-[4-(1,1-dimethylethyl)-1-cyclohexen-1-yl]-3-iodo-；1-(4-tert-butylcyclohexen-1-yl)-3-iodobenzene
• CAS: 163394-75-0
• 化学式: C₁₆H₂₁I
• 分子量: 340.247
• InChiKey: GADZVROXHHPSJF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  17
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为产物：
  描述：

  4-tert-butyl-1-cyclohexenyl(phenyl)(tetrafluoroborato)-λ³-iodane 在 四丁基氯化铵 作用下， 以 甲醇 为溶剂， 反应 3.0h， 以49%的产率得到4-叔丁基环己酮
  参考文献：
  名称：

  环己烯基四氟硼化碘与溴离子的反应：延迟由于λ的形成3 -Bromoiodane

  摘要：

  4-反应叔-butylcyclohex -1-烯基（苯基）碘鎓四氟硼酸盐（1A）和4-氯苯基衍生物（1b中与溴离子）在甲醇，乙腈，和氯仿进行了研究。产品包括衍生自中间体环己烯基阳离子以及1-溴环己烯的产品。动力学测量表明，加入的溴化物强烈阻碍了1的反应。观察到的速率常数对溴化物浓度的曲线依赖性是典型的中间体加合物的平衡前形成的过程，该中间体加合物具有不依赖溴化物的快速反应（碘鎓离子的溶剂分解）。加合物的形成，λ 3紫外光谱的变化也证实了溴代碘。碘鎓离子的相对反应性和λ 3 -bromoiodane被评估为10的量级2。溴化物取代产物既通过游离碘鎓离子的S N 1反应形成，也通过碘烷的配体偶联形成。

  DOI：

  10.1021/jo0523013

文献信息

• Solvolysis of Cyclohexenyliodonium Salt, a New Precursor for the Vinyl Cation: Remarkable Nucleofugality of the Phenyliodonio Group and Evidence for Internal Return from an Intimate Ion-Molecule Pair
  作者：Tadashi Okuyama、Tomoki Takino、Takuya Sueda、Masahito Ochiai

  DOI：10.1021/ja00117a006

  日期：1995.3

  Solvolysis of (4-tert-butyl-1-cyclohexenyl)aryliodonium tetrafluoroborates was examined in alcohol and aqueous solutions at 25-70 degrees C. Phenyliodonio group was found to be a remarkably good nucleofuge with a leaving ability about 10(6) times greater than triflate. In addition to the expected solvolysis products, 1-alkoxycyclohexene and/or cyclohexanone and iodobenzene, the internal return products, (4-tert-butyl-1-cyclohexenyl)iodobenzenes, were obtained in yields of 13-15% in methanol and aqueous solutions and of 30-40% in trifluoroethanol. The ortho derivative is the predominant isomer of these products, and this isomeric distribution is taken as indicating that the return is occurring from the intimate ion-molecule pair. The formation of a free-radical product, 4-tert-butylcyclohexene (1%), was detected during the solvolysis in the presence of 1,4-cyclohexadiene or in 2-propanol, while a considerable amount of the cationic rearrangement product, cyclopentyl methyl ketone, was obtained in the solvolysis of (2-methyl-1-cyclohexenyl)phenyliodonium tetrafluoroborate. A proposed mechanism involves mainly heterolysis to give the cyclohexenyl cation-iodobenzene pair with accompanying single electron transfer (or with competing homolysis) to lead to a free radical intermediate.
• Reactions of Cyclohexenyl Iodonium Tetrafluoroborate with Bromide Ion:  Retardation Due to the Formation of λ³-Bromoiodane
  作者：Tadashi Okuyama、Shohei Imamura、Morifumi Fujita

  DOI：10.1021/jo0523013

  日期：2006.2.1

  The reaction of 4-tert-butylcyclohex-1-enyl(phenyl)iodonium tetrafluoroborate (1a) and the 4-chlorophenyl derivative (1b) with bromide ion was examined in methanol, acetonitrile, and chloroform. Products include those derived from the intermediate cyclohexenyl cation as well as 1-bromocyclohexene. Kinetic measurements show that the reaction of 1 is strongly retarded by the added bromide. The curved

  4-反应叔-butylcyclohex -1-烯基（苯基）碘鎓四氟硼酸盐（1A）和4-氯苯基衍生物（1b中与溴离子）在甲醇，乙腈，和氯仿进行了研究。产品包括衍生自中间体环己烯基阳离子以及1-溴环己烯的产品。动力学测量表明，加入的溴化物强烈阻碍了1的反应。观察到的速率常数对溴化物浓度的曲线依赖性是典型的中间体加合物的平衡前形成的过程，该中间体加合物具有不依赖溴化物的快速反应（碘鎓离子的溶剂分解）。加合物的形成，λ 3紫外光谱的变化也证实了溴代碘。碘鎓离子的相对反应性和λ 3 -bromoiodane被评估为10的量级2。溴化物取代产物既通过游离碘鎓离子的S N 1反应形成，也通过碘烷的配体偶联形成。