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N-(triflyloxy)-N-methyl-3-methylbutanamide | 156025-81-9

中文名称
——
中文别名
——
英文名称
N-(triflyloxy)-N-methyl-3-methylbutanamide
英文别名
[Methyl(3-methylbutanoyl)amino] trifluoromethanesulfonate
N-(triflyloxy)-N-methyl-3-methylbutanamide化学式
CAS
156025-81-9
化学式
C7H12F3NO4S
mdl
——
分子量
263.238
InChiKey
NCUGZTBAKNHFNR-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):
    1.8
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    72.1
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    N-(triflyloxy)-N-methyl-3-methylbutanamide三氟化硼 作用下, 以 二氯甲烷 为溶剂, 生成 N-(3-butenyl)-3-methylbutanamide
    参考文献:
    名称:
    Generation of N-acyl iminium ions from ionization-rearrangement reactions of N-triflyloxy amides
    摘要:
    N-Triflyloxy amides undergo ionization in refluxing isopropanol to give N-acyliminium ions which can be trapped by addition of allyltrimethylsilane to the reaction mixture. Alternatively they can be converted to N-(isopropoxy)alkyl amides and then back to N-acyliminium ions under a variety of conditions.
    DOI:
    10.1016/s0040-4039(00)76872-9
  • 作为产物:
    描述:
    异戊酰氯 、 alkaline earth salt of/the/ methylsulfuric acid 在 2,6-二甲基吡啶氢氧化钾 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 2.83h, 生成 N-(triflyloxy)-N-methyl-3-methylbutanamide
    参考文献:
    名称:
    A Facile Preparation of N-(Isopropoxyalkyl) Amides by Generation and Trapping of N-Acyliminium Ions from Ionization-Rearrangement Reactions of N-Triflyloxy Amides
    摘要:
    A series of hydroxamic acids were converted to N-triflyloxy amides which were heated in 2-propanol to give N-(1-isopropoxyalkyl) amides in high yields. The method is simple, direct, and extremely tolerant of structural diversity both in the N-acyl group, as well as in the 1-isopropoxyalkyl group. N-Alkylation of secondary N-(1-isopropoxyalkyl) amides can be used for converting them to tertiary N-(1-isopropoxyalkyl) amides. N-Acyliminium ions of wide structural diversity can be generated easily from N-(1-isopropoxyalkyl) amides available by this methodology.
    DOI:
    10.1021/jo00092a007
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文献信息

  • Hoffman Robert V., Nayyar Naresh K., J. Org. Chem, 59 (1994) N 13, S 3530-3539
    作者:Hoffman Robert V., Nayyar Naresh K.
    DOI:——
    日期:——
  • Hoffman Robert V., Nayyar Naresh K., Shankweiler Jean M., Klinekole Bruce+, Tetrahedron Lett, 35 (1994) N 20, S 3231-3234
    作者:Hoffman Robert V., Nayyar Naresh K., Shankweiler Jean M., Klinekole Bruce+
    DOI:——
    日期:——
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