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1-benzyl-1,2-diphenylethylamine hydrochloride | 936647-28-8

中文名称
——
中文别名
——
英文名称
1-benzyl-1,2-diphenylethylamine hydrochloride
英文别名
1-Benzyl-1,2-diphenylethylamine hydrochloride;1,2,3-triphenylpropan-2-amine;hydrochloride
1-benzyl-1,2-diphenylethylamine hydrochloride化学式
CAS
936647-28-8
化学式
C21H21N*ClH
mdl
——
分子量
323.865
InChiKey
PHZMMDGTDRBROH-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):
    0.61
  • 重原子数:
    23
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    27.6
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    苯甲腈苄基氯化镁titanium(IV) isopropylate 盐酸 作用下, 以 乙醚二氯甲烷 为溶剂, 以64%的产率得到1-benzyl-1,2-diphenylethylamine hydrochloride
    参考文献:
    名称:
    Addition of organometallic reagents to nitriles promoted by titanium(IV) isopropoxide as a procedure of synthesis of primary tert-alkylamines
    摘要:
    Grignard reagents are able to add twice to nitriles in the presence of titanium(IV) isopropoxide providing primary tert-alkylamines in a fair yield. The conditions and structural features of reagents required for successful reaction were established. A possibility to apply two different organometallic reagents was demonstarated, in particular, the use of organolithium compounds in the second stage.
    DOI:
    10.1134/s1070428007100016
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文献信息

  • US3992370A
    申请人:——
    公开号:US3992370A
    公开(公告)日:1976-11-16
  • Addition of organometallic reagents to nitriles promoted by titanium(IV) isopropoxide as a procedure of synthesis of primary tert-alkylamines
    作者:O. A. Tomashenko、V. V. Sokolov、A. A. Tomashevskii、A. A. Potekhin、A. de Meijere
    DOI:10.1134/s1070428007100016
    日期:2007.10
    Grignard reagents are able to add twice to nitriles in the presence of titanium(IV) isopropoxide providing primary tert-alkylamines in a fair yield. The conditions and structural features of reagents required for successful reaction were established. A possibility to apply two different organometallic reagents was demonstarated, in particular, the use of organolithium compounds in the second stage.
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