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N-(tert-butyldimethylsilyl)aminomorpholine | 1413917-28-8

中文名称
——
中文别名
——
英文名称
N-(tert-butyldimethylsilyl)aminomorpholine
英文别名
——
N-(tert-butyldimethylsilyl)aminomorpholine化学式
CAS
1413917-28-8
化学式
C10H24N2OSi
mdl
——
分子量
216.399
InChiKey
JSWKETKEEVBVTH-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):
    1.83
  • 重原子数:
    14.0
  • 可旋转键数:
    2.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    24.5
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    N-(tert-butyldimethylsilyl)aminomorpholine对硝基苯甲醛氘代氯仿 为溶剂, 反应 192.0h, 以8%的产率得到N-morpholino-1-(4-nitrophenyl)methanimine
    参考文献:
    名称:
    N-Silyloxaziridines: Synthesis and Use for Electrophilic Amination
    摘要:
    N-Silyloxaziridines were synthesized for the first time. Their tert-butyldiphenylsilyl (TBDPS) derivatives were stable reagents that were prepared on a multigram scale in three steps and in 44% overall yield from the corresponding benzylamines. They were mild electrophilic aminating reagents that reacted at room temperature with diversely substituted primary and secondary amines to produce N-monoalkyl or N,N-dialkyl benzaldehyde hydrazones in 44-87% yield.
    DOI:
    10.1021/jo302182t
  • 作为产物:
    描述:
    4-氨基吗啉叔丁基二甲基氯硅烷4-二甲氨基吡啶三乙胺 作用下, 以 乙醚 为溶剂, 反应 48.0h, 以66%的产率得到N-(tert-butyldimethylsilyl)aminomorpholine
    参考文献:
    名称:
    N-Silyloxaziridines: Synthesis and Use for Electrophilic Amination
    摘要:
    N-Silyloxaziridines were synthesized for the first time. Their tert-butyldiphenylsilyl (TBDPS) derivatives were stable reagents that were prepared on a multigram scale in three steps and in 44% overall yield from the corresponding benzylamines. They were mild electrophilic aminating reagents that reacted at room temperature with diversely substituted primary and secondary amines to produce N-monoalkyl or N,N-dialkyl benzaldehyde hydrazones in 44-87% yield.
    DOI:
    10.1021/jo302182t
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