(2-溴乙基)苯-D5 | 35845-64-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: (2-溴乙基)苯-D5
• 英文名称: 2-pentadeuterophenylethyl bromide
• 英文别名: [phenyl-2H5]phenethyl alcohol；(2-bromo-ethyl)-pentadeuterio-benzene；2-<²H5>Phenylaethylbromid；(2-Bromoethyl)benzene-D5；1-(2-bromoethyl)-2,3,4,5,6-pentadeuteriobenzene
• CAS: 35845-64-8
• 化学式: C₈H₉Br
• 分子量: 190.024
• InChiKey: WMPPDTMATNBGJN-RALIUCGRSA-N

物化性质

• 溶解度：
  氯仿（微溶）、乙酸乙酯（微溶）

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  9
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.25
• 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：

  (2-溴乙基)苯-D5 在 magnesium 作用下， 生成 3-(<(2)H5>phenyl)propanoic acid
  参考文献：
  名称：

  On the generation and characterization of the spiro[2,5]octadienyl anion in the gas phase

  摘要：

  AbstractThree routes have been explored in both a high‐pressure chemical ionization (CI) source and a low‐pressure Fourier transform ion cyclotron resonance (FT‐ICR) cell to generate the spiro[2,5]octadienyl anion in the gas phase: (i) proton abstraction from spiro[2,5]octa‐4,6‐diene; (ii) expulsion of trimethysilyl fluoride by phenyl ring participation following fluoride anion attack upon the silicon centre of 2‐phenylethyl trimethylsilane; and (iii) collisionally induced dissociation (CID) of the carboxylate anion of 3‐phenylpropanoic acid via carbon dioxide loss. From comparison of the CID spectra of various reference [C8H9]− ions with those of the [C8H9]− ions which could be generated via the routes (i) and (iii) in the CI source it can be concluded that only the third route yields a [C8H9]−ion whose CID spectrum is not inconsistent with the one expected for the spiro[2,5]octadienyl anion. In the FT‐ICR cell [C8H9]− ions are generated along all three routes; their structures have been identified by specific ion‐molecule reactions and appear to be different. Route (i) yields an α‐methyl benzyl anion, probably due to isomerization within the ion‐molecule complex formed. An ortho‐ethylphenyl anion is formed along route (ii), presumably due to an intramolecular ortho proton abstraction in the generated trimethylsilyl fluoride solvated 2‐phenylethyl primary carbanion. The [C8H9]− ion formed along route (iii) shows reactions similar to those of the 1,1‐dimethylcyclohexadienyl anion which is structurally related to the spiro[2,5]octadienyl anion. Furthermore, the [C8H9]− ion generated via route (iii) reacts with hexafluorobenzene under expulsion of only one hydrogen fluoride molecule which contains exclusively one of the original phenyl ring hydrogen atoms. On the basis of all these observations it is therefore quite likely that the spiro[2,5]octadienyl anion is formed by collisionally induced decarboxylation of the 3‐phenylpropanoic acid carboxylate anion and can be a long‐lived and stable species in the gas phase.

  DOI：

  10.1002/oms.1210240807
• 作为产物：
  描述：

  Phenyl-d5-magnesium bromide 在 三溴化磷 作用下， 生成 (2-溴乙基)苯-D5
  参考文献：
  名称：

  On the generation and characterization of the spiro[2,5]octadienyl anion in the gas phase

  摘要：

  AbstractThree routes have been explored in both a high‐pressure chemical ionization (CI) source and a low‐pressure Fourier transform ion cyclotron resonance (FT‐ICR) cell to generate the spiro[2,5]octadienyl anion in the gas phase: (i) proton abstraction from spiro[2,5]octa‐4,6‐diene; (ii) expulsion of trimethysilyl fluoride by phenyl ring participation following fluoride anion attack upon the silicon centre of 2‐phenylethyl trimethylsilane; and (iii) collisionally induced dissociation (CID) of the carboxylate anion of 3‐phenylpropanoic acid via carbon dioxide loss. From comparison of the CID spectra of various reference [C8H9]− ions with those of the [C8H9]− ions which could be generated via the routes (i) and (iii) in the CI source it can be concluded that only the third route yields a [C8H9]−ion whose CID spectrum is not inconsistent with the one expected for the spiro[2,5]octadienyl anion. In the FT‐ICR cell [C8H9]− ions are generated along all three routes; their structures have been identified by specific ion‐molecule reactions and appear to be different. Route (i) yields an α‐methyl benzyl anion, probably due to isomerization within the ion‐molecule complex formed. An ortho‐ethylphenyl anion is formed along route (ii), presumably due to an intramolecular ortho proton abstraction in the generated trimethylsilyl fluoride solvated 2‐phenylethyl primary carbanion. The [C8H9]− ion formed along route (iii) shows reactions similar to those of the 1,1‐dimethylcyclohexadienyl anion which is structurally related to the spiro[2,5]octadienyl anion. Furthermore, the [C8H9]− ion generated via route (iii) reacts with hexafluorobenzene under expulsion of only one hydrogen fluoride molecule which contains exclusively one of the original phenyl ring hydrogen atoms. On the basis of all these observations it is therefore quite likely that the spiro[2,5]octadienyl anion is formed by collisionally induced decarboxylation of the 3‐phenylpropanoic acid carboxylate anion and can be a long‐lived and stable species in the gas phase.

  DOI：

  10.1002/oms.1210240807

文献信息

• The synthesis of [phenyl-2H5]gluconasturtiin and its metabolites for metabolic studies
  作者：John J. Morrison、Nigel P. Botting

  DOI：10.1002/jlcr.1004

  日期：2005.10.30

  The synthesis of a deuterium labelled glucosinolate, [2H5]gluconasturtiin, is described starting from [2H5]bromobenzene. The potential metabolites of the glucosinolate, namely the [phenyl-2H5]phenethyl isothiocyanate, nitrile, thiocyanate, amine and the mercapturic acid conjugate of phenethyl isothiocyanate are also described. This series of compounds has been prepared for use in feeding studies to

  描述了从 [2H5] 溴苯开始合成氘标记的芥子油苷，[2H5]gluconasturtiin。还描述了硫代葡萄糖苷的潜在代谢物，即 [苯基-2H5] 苯乙基异硫氰酸酯、腈、硫氰酸酯、胺和苯乙基异硫氰酸酯的巯基酸共轭物。该系列化合物已制备用于喂养研究，以检查葡糖苷酸的哺乳动物代谢并寻找新的暴露生物标志物。版权所有 © 2005 John Wiley & Sons, Ltd.
• Intramolecular ring-to-ring proton transfer in gaseous (.omega.-phenylalkyl)benzenium ions
  作者：Dietmar Kuck、Wolfgang Baether、Hans Friedrich Gruetzmacher

  DOI：10.1021/ja00518a004

  日期：1979.11

  corresponding 1 -(a-phenylalkyl)- 1,4-dihydrobenzoic acids 4 and 5. The major secondary fragmentation is loss of benzene from 1 and 2. It is shown by deuterium labeling that 1 and 2 ions undergo repeated ring-to-ring proton transfer reactions, equilibrating all of the 11 "aromatic" hydrogen atoms within s without involving those from the aliphatic chain. A competition between the ring-to-ring (quasi-intermolecular)

  气态（2-苯基乙基）苯鎓和（3-苯基1丙基）苯鎓离子 1 和 2 很容易通过质谱损失从相应的 1-（α-苯基烷基）- 1,4-二氢苯甲酸的正分子离子中的 CO2H 生成酸 4 和 5。主要的二次碎裂是苯从 1 和 2 的损失。氘标记表明 1 和 2 离子经历重复的环到环质子转移反应，平衡了所有 11 个“芳香”氢原子在 s 内，不涉及脂肪链中的那些。讨论了环到环（准分子间）质子转移和环内质子转移（“环行走”）之间的竞争。