3-bromo-1-(chloromethyl)bicyclo<1.1.1>pentane | 137741-18-5

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 有机氯化物
• 英文名称: 3-bromo-1-(chloromethyl)bicyclo<1.1.1>pentane
• 英文别名: 1-Bromo-3-(chloromethyl)bicyclo[1.1.1]pentane
• CAS: 137741-18-5
• 化学式: C₆H₈BrCl
• 分子量: 195.487
• InChiKey: GMTGSQOHLPRTOA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  8
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  3-bromo-1-(chloromethyl)bicyclo<1.1.1>pentane 在 水 作用下， 以 乙醇 为溶剂， 生成 1-(chloromethyl)-3-methylene-1-cyclobutanol
  参考文献：
  名称：

  溶剂分解3-取代的双环[1.1.1]戊基溴化物中的感应电荷分散

  摘要：

  3-取代的双环[1.1.1]戊基溴化物的溶剂分解速率和产物表明，在离子化为双环[1.1.1]戊基-1-阳离子（3-亚甲基环丁醇的前体）的过程中，极强的感应电荷分散。

  DOI：

  10.1016/s0040-4039(00)79433-0
• 作为产物：
  描述：

  2-thioxo-1,2-dihydropyridin-1-yl 3-(methoxycarbonyl)bicyclo<1.1.1>pentane-1-carboxylate 在 吡啶 、 lithium aluminium tetrahydride 、 氟烷 、 lithium chloride 作用下， 以 四氢呋喃 、 乙醚 、 二氯甲烷 为溶剂， 反应 86.0h， 生成 3-bromo-1-(chloromethyl)bicyclo<1.1.1>pentane
  参考文献：
  名称：

  Synthesis of Some Bridgehead-Bridgehead-Disubstituted Bicyclo[1.1.1]pentanes

  摘要：

  The synthesis of a wide variety of 1,3-disubstituted bicyclo[1.1.1]pentanes is described, with particular emphasis on the generation of a series of S-X-substituted bicyclo[1.1.1]pentyl bromides required for solvolytic studies. Functional group manipulation at the bridgehead was readily accomplished in the majority of cases by radical processes in some instances, transformations were effected via carbanionic-type intermediates.

  DOI：

  10.1021/jo00090a015

文献信息

• Inductive charge dispersal in the solvolysis of 3-substituted bicyclo[1.1.1] pentyl bromides
  作者：Cyril A. Grob、Cheng Xi Yang、Ernest W. Della、Dennis K. Taylor

  DOI：10.1016/s0040-4039(00)79433-0

  日期：1991.10

  Solvolysis rates and products of 3-substituted bicyclo[1.1.1]pentyl bromides indicate extremely strong inductive charge dispersal in the ionization to bicyclo[1.1.1]pentyl-1-cations, the precursors of 3-methylenecyclobutanols.

  3-取代的双环[1.1.1]戊基溴化物的溶剂分解速率和产物表明，在离子化为双环[1.1.1]戊基-1-阳离子（3-亚甲基环丁醇的前体）的过程中，极强的感应电荷分散。
• Della Ernest W., Taylor Dennis K., J. Org. Chem, 59 (1994) N 11, S 2986-2996
  作者：Della Ernest W., Taylor Dennis K.

  DOI：——

  日期：——
• Bridgehead Carbocations: A Solvolytic Study of 1-Bromobicyclo[1.1.1]pentane and Its Bridgehead-Substituted Derivatives
  作者：Ernest W. Della、Cyril A. Grob、Dennis K. Taylor

  DOI：10.1021/ja00093a014

  日期：1994.7

  The rate constants (k) for solvolysis of a range of 3-X-substituted bicyclo[1.1.1]pentyl bromides in 80% aqueous ethanol have been measured and a linear relationship found to exist between log k and the inductive/field constant sigma(I). These observations, together with the results of isotope and solvent effect studies described below, have been interpreted as evidence for the formation of 1-bicyclo[1.1.1]pentyl cations in the ionization step in preference to mechanisms in which either ring-opening is concerted with ionization to give 3-methylenecyclobutyl cations or ionization is accompanied by ring-contraction to give bicyclo[1.1.0]butyl-1-carbinyl cations. The latter mechanisms would have been expected to show the effects of strong pi-donor substituent participation, a phenomenon which was not observed. A comparison of the rates of solvolysis of the parent bromide and its 3-deuterated analog is characterized by a large deuterium-isotope effect (k(H)/k(D) = 1.30) which, combined with the observation that 1-bromobicyclo[1.1.1]pentane solvolyses with enhanced rates in solvents which are strong hydrogen bonding accepters, lends support to the view that the 1-bicyclo[1.1.1]pentyl cation derives substantial stabilization from sigma-hyperconjugative interactions.
• Synthesis of Some Bridgehead-Bridgehead-Disubstituted Bicyclo[1.1.1]pentanes
  作者：Ernest W. Della、Dennis K. Taylor

  DOI：10.1021/jo00090a015

  日期：1994.6

  The synthesis of a wide variety of 1,3-disubstituted bicyclo[1.1.1]pentanes is described, with particular emphasis on the generation of a series of S-X-substituted bicyclo[1.1.1]pentyl bromides required for solvolytic studies. Functional group manipulation at the bridgehead was readily accomplished in the majority of cases by radical processes in some instances, transformations were effected via carbanionic-type intermediates.