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N,N-diallyl-2,2-dimethylpropanamide | 60901-59-9

中文名称
——
中文别名
——
英文名称
N,N-diallyl-2,2-dimethylpropanamide
英文别名
tert-butyl N,N-diallylcarbamate;N,N-Diallylpivalamide;2,2-dimethyl-N,N-bis(prop-2-enyl)propanamide
N,N-diallyl-2,2-dimethylpropanamide化学式
CAS
60901-59-9
化学式
C11H19NO
mdl
MFCD03375926
分子量
181.278
InChiKey
DUBSFCBNHNWHDY-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

物化性质

  • 沸点:
    251.8±29.0 °C(Predicted)
  • 密度:
    0.885±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    13
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.545
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    N,N-diallyl-2,2-dimethylpropanamidelithium 作用下, 反应 1.0h, 以50%的产率得到2,2-二甲基己-5-烯-3-酮
    参考文献:
    名称:
    Generation of allylic and benzylic organolithium reagents from the corresponding ester, amide, carbonate, carbamate and urea derivatives
    摘要:
    The reaction of different allylic and benzylic non-enolisable esters or amides (1), carbonates (4), carbamates (6, 7) and ureas (8) with an excess of lithium powder and a catalytic amount of naphthalene (10%) in the presence of an electrophile [iPrCHO, tBuCHO, PhCHO, Me2CO, Et2CO, (CH2)(5)CO, Ph2CO, MeSiCl] in THF at different temperatures (-78, -30 or 0 degrees C) leads, after hydrolysis with water, to the corresponding allylated or benzylated products (2). (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(99)00610-9
  • 作为产物:
    描述:
    三甲基乙酰氯二烯丙基胺三乙胺 作用下, 以89%的产率得到N,N-diallyl-2,2-dimethylpropanamide
    参考文献:
    名称:
    Generation of allylic and benzylic organolithium reagents from the corresponding ester, amide, carbonate, carbamate and urea derivatives
    摘要:
    The reaction of different allylic and benzylic non-enolisable esters or amides (1), carbonates (4), carbamates (6, 7) and ureas (8) with an excess of lithium powder and a catalytic amount of naphthalene (10%) in the presence of an electrophile [iPrCHO, tBuCHO, PhCHO, Me2CO, Et2CO, (CH2)(5)CO, Ph2CO, MeSiCl] in THF at different temperatures (-78, -30 or 0 degrees C) leads, after hydrolysis with water, to the corresponding allylated or benzylated products (2). (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(99)00610-9
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文献信息

  • Novel Tetrahydro-1H-Pyrido[4,3-b] Indole Derivatives as CB1 Receptor Ligands
    申请人:Cheng Yun-Xing
    公开号:US20100113502A1
    公开(公告)日:2010-05-06
    Compounds of formulae I, or pharmaceutically acceptable salts thereof: wherein R 1 , R 2 and R 3 are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.
    化合物I的公式,或其药学上可接受的盐:其中R1、R2和R3如规范中所定义,以及包括这些化合物的盐和药物组合物已被制备。它们在治疗中很有用,特别是在疼痛管理方面。
  • Hoveyda–Grubbs first generation type catalyst immobilized on mesoporous molecular sieves
    作者:Jakub Pastva、Jiří Čejka、Naděžda Žilková、Oto Mestek、Mojca Rangus、Hynek Balcar
    DOI:10.1016/j.molcata.2013.06.006
    日期:2013.11
    New heterogeneous, reusable catalysts for olefin metathesis have been prepared by immobilizing the Hoveyda-Grubbs first generation type alkylidene (commercially available as the Zhan catalyst-1C) on siliceous mesoporous molecular sieves with different pore sizes and architectures (SBA-15, SBA-16, MCM-41 and MCM-48) having the surface modified with molecules bearing dicyclohexylphosphine (PCy2) end groups. Resulting novel heterogenized catalysts proved high activity in ring-closing metathesis (RCM) of 1,7-octadiene, diethyl diallylmalonate, tert-butyl N,N-diallylcarbamate and N,N-diallyl-2,2,2-trifluoroacetamide, in homometathesis of 1-decene, 5-hexenyl acetate and methyl 10-undecenoate, and in cross-metathesis (CM) of allylbenzene with cis-1,4-diacetoxy-2-butene. The catalytic activity decreased with decreasing pore size of supports in the order SBA-15 > MCM-48 > SBA-16 and MCM-41. Filtration test suggested that the solid catalyst was responsible for the catalytic activity. Catalysts were easily separated from the reaction mixtures and products of low levels of Ru concentration were obtained. (c) 2013 Elsevier B.V. All rights reserved.
  • Krompiec; Suwinski; Grobelny, Polish Journal of Chemistry, 1997, vol. 71, # 6, p. 747 - 753
    作者:Krompiec、Suwinski、Grobelny、Wagner
    DOI:——
    日期:——
  • Krompiec; Suwinski; Gibas, Polish Journal of Chemistry, 1996, vol. 70, # 1, p. 133 - 134
    作者:Krompiec、Suwinski、Gibas、Grobelny
    DOI:——
    日期:——
  • Structure elucidation of a zwitterionic 2-oxazoline obtained by cyclofunctionalization of n-acetyldiallylamine with tellurium tetrachloride
    作者:Jan Bergman、Jan Sidén、Knut Maartmann-Moe
    DOI:10.1016/s0040-4020(01)91812-5
    日期:1984.1
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