2-benzyl-4-bromobenzaldehyde | 1075741-03-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-benzyl-4-bromobenzaldehyde
• CAS: 1075741-03-5
• 化学式: C₁₄H₁₁BrO
• 分子量: 275.145
• InChiKey: RQRJCBNZDMVJJM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 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：

  2-benzyl-4-bromobenzaldehyde 、 9-(3-phenylpropyl)-9-borabicyclo[3.3.1]nonane 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 sodium hydroxide 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 12.0h， 以0.700 g的产率得到2-benzyl-4-(3-phenylpropyl)benzaldehyde
  参考文献：
  名称：

  Potential Modes of Interaction of 9-Aminomethyl-9,10-dihydroanthracene (AMDA) Derivatives with the 5-HT_2A Receptor: A Ligand Structure-Affinity Relationship, Receptor Mutagenesis and Receptor Modeling Investigation

  摘要：

  The effects of 3-position substitution of 9-aminomethyl-9,10-dihydroanthracene (AMDA) on 5-HT2A receptor affinity were determined and compared to a parallel series of DOB-like 1-(2,5-dimethoxyphenyl)-2-aminopropanes substituted at the 4-position. The results were interpreted within the context of 5-HT2A receptor models that suggest that members of the DOB-like series call bind to the receptor in two distinct modes that correlate with the compounds' functional activity. Automated ligand docking and molecular dynamics suggest that all of the AMDA derivatives, the parent of which is a 5-HT2A antagonist, bind in a fashion analogous to that for the sterically demanding antagonist DOB-like compounds. The failure of the F340(6.52)L mutation to adversely affect the affinity of AMDA and the 3-bromo derivative is consistent with the proposed modes of orientation. Evaluation of ligand-receptor complex models suggest that a valine/threonine exchange between the 5-HT2A and D-2 receptors may be the origin of selectivity for AMDA and two substituted derivatives.

  DOI：

  10.1021/jm800771x
• 作为产物：
  描述：

  2-benzyl-4-bromobenzyl alcohol 在 silica gel 、 pyridinium chlorochromate 作用下， 以 二氯甲烷 为溶剂， 以0.750 g的产率得到2-benzyl-4-bromobenzaldehyde
  参考文献：
  名称：

  Potential Modes of Interaction of 9-Aminomethyl-9,10-dihydroanthracene (AMDA) Derivatives with the 5-HT_2A Receptor: A Ligand Structure-Affinity Relationship, Receptor Mutagenesis and Receptor Modeling Investigation

  摘要：

  The effects of 3-position substitution of 9-aminomethyl-9,10-dihydroanthracene (AMDA) on 5-HT2A receptor affinity were determined and compared to a parallel series of DOB-like 1-(2,5-dimethoxyphenyl)-2-aminopropanes substituted at the 4-position. The results were interpreted within the context of 5-HT2A receptor models that suggest that members of the DOB-like series call bind to the receptor in two distinct modes that correlate with the compounds' functional activity. Automated ligand docking and molecular dynamics suggest that all of the AMDA derivatives, the parent of which is a 5-HT2A antagonist, bind in a fashion analogous to that for the sterically demanding antagonist DOB-like compounds. The failure of the F340(6.52)L mutation to adversely affect the affinity of AMDA and the 3-bromo derivative is consistent with the proposed modes of orientation. Evaluation of ligand-receptor complex models suggest that a valine/threonine exchange between the 5-HT2A and D-2 receptors may be the origin of selectivity for AMDA and two substituted derivatives.

  DOI：

  10.1021/jm800771x

文献信息

• Semicarbazide: A Transient Directing Group for C( <i>sp</i> ³ )−H Arylation of 2‐Methylbenzaldehydes
  作者：Fei Wen、Zheng Li

  DOI：10.1002/adsc.201901392

  日期：2020.1.7

  Semicarbazide as an effective transient directing group for C(sp3)−H arylation of 2‐methylbenzaldehydes is described. Various substituted 2‐benzylbenzaldehydes are efficiently synthesized by this strategy. The salient features of this protocol are the use of inexpensive transient directing group, wide scope of substrates with good functional group compatibility, up to 98% yield, and applicability to

  氨基脲是2-甲基苯甲醛的C（sp 3）-H芳基化的有效瞬态导向基团。通过这种策略可以有效地合成各种取代的2-苄基苯甲醛。该协议的显着特征是使用廉价的瞬态导向基团，具有良好的官能团相容性，高达98％的收率以及适用于克规模的底物范围广。
• Palladium-catalyzed benzylic C(sp3)–H arylation of o-alkylbenzaldehydes
  作者：Lan Lei、Ping Wu、Zhuqing Liu、Jiang Lou

  DOI：10.1016/j.tetlet.2021.152865

  日期：2021.3

  The palladium-catalyzed benzylic C(sp3)–H arylation of o-alkylbenzaldehyde derivatives was achieved utilizing 2-dimethylaminoethylamine as a novel transient directing group. The γ-C(sp3)–H arylation reaction efficiently afforded a variety of arylated o-alkylbenzaldehydes and polycyclic aromatic hydrocarbons (PAHs) in one pot, exhibiting high functional group tolerance with broad substrate scope. The

  钯催化的邻烷基苯甲醛衍生物的苄基C（SP 3）-H芳基化反应是利用2-二甲基氨基乙胺作为新型的瞬态导向基团实现的。的γ -C（SP 3）-H的芳基化反应有效地得到各种芳基化Ó以一个锅煮-alkylbenzaldehydes和多环芳香烃（PAHs），表现出与广泛的底物范围高的官能团耐受性。脂族二胺助剂代表用于C H活化的简单，廉价，易于获得和可除去的导向基团。结果o在温和的条件下，可以将苄基苯甲醛产品多样化地转化为潜在重要的合成中间体。