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1-dimethylamino-trans-2,6-dimethylpiperidine

中文名称
——
中文别名
——
英文名称
1-dimethylamino-trans-2,6-dimethylpiperidine
英文别名
——
1-dimethylamino-trans-2,6-dimethylpiperidine化学式
CAS
——
化学式
C9H20N2
mdl
——
分子量
156.271
InChiKey
IHCBRMTWGXELFD-RKDXNWHRSA-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):
    1.73
  • 重原子数:
    11.0
  • 可旋转键数:
    1.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    6.48
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为产物:
    描述:
    2,6-庚二酮偏二甲肼氢氧化钾三乙酰氧基硼氢化钠溶剂黄146 作用下, 以 乙腈 为溶剂, 以10%的产率得到3-甲基-2-环己烯-1-酮
    参考文献:
    名称:
    Diastereoselective synthesis of 2,5-dimethylpyrrolidines and 2,6-dimethylpiperidines by reductive amination of 2,5-hexanedione and 2,6-heptanedione with hydride reagents
    摘要:
    The reductive amination of 2,5-hexanedione and 2,6-heptanedione with ammonia and primary amines in the presence of hydride reagents afforded 2,5-dimethylpyrrolidines and 2,6-dimethylpiperidines with variable diastereoselectivity, as the cis/trans ratio was affected by the size of the ring formed and the steric and electronic properties of the nitrogen substituent. Increasing the bulkiness of the nitrogen substituent, the cis pyrrolidines and the bans-piperidines were obtained with enhanced selectivity.
    DOI:
    10.1016/s0040-4020(01)85010-9
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文献信息

  • Diastereoselective synthesis of 2,5-dimethylpyrrolidines and 2,6-dimethylpiperidines by reductive amination of 2,5-hexanedione and 2,6-heptanedione with hydride reagents
    作者:Carla Boga、Francesco Manescalchi、Diego Savoia
    DOI:10.1016/s0040-4020(01)85010-9
    日期:1994.4
    The reductive amination of 2,5-hexanedione and 2,6-heptanedione with ammonia and primary amines in the presence of hydride reagents afforded 2,5-dimethylpyrrolidines and 2,6-dimethylpiperidines with variable diastereoselectivity, as the cis/trans ratio was affected by the size of the ring formed and the steric and electronic properties of the nitrogen substituent. Increasing the bulkiness of the nitrogen substituent, the cis pyrrolidines and the bans-piperidines were obtained with enhanced selectivity.
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