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2,2-dibenzyl-1,3-dichloropropane | 208725-46-6

中文名称
——
中文别名
——
英文名称
2,2-dibenzyl-1,3-dichloropropane
英文别名
2,2-bis(benzyl)-1,3-dichloropropane;[2-Benzyl-3-chloro-2-(chloromethyl)propyl]benzene
2,2-dibenzyl-1,3-dichloropropane化学式
CAS
208725-46-6
化学式
C17H18Cl2
mdl
——
分子量
293.236
InChiKey
BNFJAVBJHSLNJP-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    19
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2,2-dibenzyl-1,3-dichloropropane 在 samarium diiodide 作用下, 以 四氢呋喃 为溶剂, 反应 48.0h, 以69%的产率得到1,1-dibenzylcyclopropane
    参考文献:
    名称:
    Radical 3-exo-tet cyclization of 1,3-dihalopropanes with SmI2 to form cyclopropanes
    摘要:
    The preparation of 1,1-disubstituted and monosubstituted cycloproparres from corresponding 2,2-disubstituted and 2-monosubstituted 1,3-dihalopropanes, respectively, with SMI2 in THF was efficiently carried out. The reaction mechanism was proposed to proceed in a radical 3-exo-tet manner based on Baldwin's rule. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.05.081
  • 作为产物:
    描述:
    参考文献:
    名称:
    Radical 3-exo-tet cyclization of 1,3-dihalopropanes with SmI2 to form cyclopropanes
    摘要:
    The preparation of 1,1-disubstituted and monosubstituted cycloproparres from corresponding 2,2-disubstituted and 2-monosubstituted 1,3-dihalopropanes, respectively, with SMI2 in THF was efficiently carried out. The reaction mechanism was proposed to proceed in a radical 3-exo-tet manner based on Baldwin's rule. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.05.081
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文献信息

  • Formation of Cyclopropanes by the Reductive Coupling of 1,3-Dihalides Promoted by Titanocene(II) Species
    作者:Takeshi Takeda、Keiko Shimane、Tooru Fujiwara、Akira Tsubouchi
    DOI:10.1246/cl.2002.290
    日期:2002.3
    The treatment of various 1,3-dihalides including the ones bearing an ester group with the titanocene(II) species produced cyclopropanes in good yields. The reaction of dihalides possessing two secondary halogens proceeded stereoselectively to afford trans-isomers as major products.
    各种含酯基的1,3-二卤化物及其他1,3-二卤化物的处理方法与二茂钛(II)物种发生反应,能够以良好的产率生成环丙烷。具有两个二级卤素的二卤化物的反应立体选择性地进行,主要产物为反式异构体。
  • 1,3-DIPHOSPHINOPROPANE LIGANDS AND TRANSITION METAL COMPLEXES FORMED THEREFROM, THEIR PREPARATION AND USE
    申请人:CONSIGLIO NAZIONALE DELLE RICERCHE
    公开号:EP0941230B1
    公开(公告)日:2004-05-12
  • Radical 3-exo-tet cyclization of 1,3-dihalopropanes with SmI2 to form cyclopropanes
    作者:Tsuyoshi Ohkita、Yuhsuke Tsuchiya、Hideo Togo
    DOI:10.1016/j.tet.2008.05.081
    日期:2008.7
    The preparation of 1,1-disubstituted and monosubstituted cycloproparres from corresponding 2,2-disubstituted and 2-monosubstituted 1,3-dihalopropanes, respectively, with SMI2 in THF was efficiently carried out. The reaction mechanism was proposed to proceed in a radical 3-exo-tet manner based on Baldwin's rule. (c) 2008 Elsevier Ltd. All rights reserved.
  • 3-exo-tet Cyclization of 2,2-disubstituted 1,3-dihalopropanes with indium in aqueous and ionic liquid solvent system
    作者:Yuhsuke Tsuchiya、Yuhta Izumisawa、Hideo Togo
    DOI:10.1016/j.tet.2009.06.123
    日期:2009.9
    The 3-exo-tet cyclization of 2,2-disubstituted 1,3-dihalopropanes with In powder in THF solution of 20% H2O, dioxane solution of 20% H2O, and ionic liquids, such as [bmim]Br, [bmim]Cl, and [bmin]BF4, respectively, was efficiently carried out to form the corresponding 1,1-disubstituted cyclopropanes in good yields. The cyclopropanation of 2,2-disubstituted 1,3-dihalopropanes with In powder in ionic liquids, such as [bmim]Br, [bmim]Cl, and [bmin]BF4, was markedly accelerated compared with that in a THF solution of 20% H2O and a dioxane solution of 20% H2O. The mechanism was proposed to involve the radical 3-exo-tet cyclization of the formed 3-halopropyl radical. (C) 2009 Elsevier Ltd. All rights reserved.
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