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N,N-diethyl-6-heptenamide | 141192-59-8

中文名称
——
中文别名
——
英文名称
N,N-diethyl-6-heptenamide
英文别名
6-Heptenamide, N,N-diethyl-;N,N-diethylhept-6-enamide
N,N-diethyl-6-heptenamide化学式
CAS
141192-59-8
化学式
C11H21NO
mdl
——
分子量
183.294
InChiKey
MYEYHXSVGKDUBP-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:
    274.3±19.0 °C(Predicted)
  • 密度:
    0.874±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:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:469d8367f5663db55c85f386a712edaa
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反应信息

  • 作为反应物:
    描述:
    N,N-diethyl-6-heptenamide2,4,6-三甲基吡啶 作用下, 以 二氯甲烷 为溶剂, 反应 15.0h, 以44%的产率得到N,N-diethyl-2-iodohept-6-enamide
    参考文献:
    名称:
    A facile α-iodination reaction of unsaturated amides
    摘要:
    A novel and mild alpha-iodination of carboxamides was developed. Unsaturated amides could be converted to the alpha-iodoamides in moderate to good yields by treatment with I2 in the presence of s-collidine.
    DOI:
    10.1016/s0040-4039(00)91606-x
  • 作为产物:
    参考文献:
    名称:
    α-酰胺自由基反应的绝对速率常数。
    摘要:
    1-(二乙基氨基甲酰基)-6,6-二苯基-5-己烯基(4a),1-(二乙基氨基甲酰基)-7,7-二苯基-6-庚烯基(4b)和1-(二乙基氨基甲酰基)-通过激光闪光光解法由相应的PTOC酯(羧酸和N-羟基吡啶-2-硫酮的酸酐)制得1-甲基-6,6-二苯基-5-己烯基(4c)。在各种温度下测量自由基4a和4b的环化动力学,并在环境温度下测量4c的环化动力学。自由基4a和4b在间接动力学研究中用作自由基钟,以确定仲α-酰胺自由基与Bu(3)SnH反应的速率常数。然后将校准的氢化锡捕获反应用于确定1-(二乙基氨基甲酰基)-5-己烯基(12)环化的速率常数。仲α-酰胺基的5-exo环化的速率常数与其同构烷基自由基类似物的速率常数相似。叔α-酰胺基团4c的5-exo环化和仲α-酰胺基团4b的6-exo环化的速率常数小于类似的烷基和α-酯取代的基团的速率常数效果。仲α-酰胺自由基的氢化锡捕获速率常数类似
    DOI:
    10.1021/jo9717907
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文献信息

  • A Sulfoxide-Promoted, Catalytic Method for the Regioselective Synthesis of Allylic Acetates from Monosubstituted Olefins via C−H Oxidation
    作者:Mark S. Chen、M. Christina White
    DOI:10.1021/ja039107n
    日期:2004.2.1
    promote C-H oxidation versus Wacker oxidation chemistry and to control the regioselectivity in the C-H oxidation products. A catalytic method for the direct C-H oxidation of monosubstituted olefins to linear (E)-allylic acetates in high regio- and stereoselectivities and preparatively useful yields is described. The method using benzoquinone as the stoichiometric oxidant and 10 mol % of Pd(OAc)2 or Pd(O2CCF3)2
    亚砜与 Pd(II) 盐的连接显示出选择性促进 CH 氧化与 Wacker 氧化化学相比,并控制 CH 氧化产物中的区域选择性。描述了一种用于将单取代烯烃直接 CH 氧化成线性 (E)-烯丙基乙酸酯的催化方法,该方法具有高区域选择性和立体选择性以及制备性有用的产率。发现使用苯醌作为化学计量氧化剂和 10 mol% Pd(OAc)2 或 Pd(O2CCF3)2 作为催化剂在 DMSO/AcOH (1:1) 溶液中的方法与广泛的官能度兼容(例如,酰胺、氨基甲酸酯、酯和醚,参见表 2)。发现添加 DMSO 对促进 CH 氧化途径至关重要,单独使用 AcOH 或与多种介电介质结合使用,导致混合物有利于瓦克型氧化产物(表 1,S3)。为了探索 DMSO 作为配体的作用,形成了双亚砜 Pd(OAc)2 络合物 1,发现它是一种有效的 CH 氧化催化剂,在不存在 DMSO 的情况下(方程式 2、3)。此外,催化剂
  • Serial Ligand Catalysis:  A Highly Selective Allylic C−H Oxidation
    作者:Mark S. Chen、Prabagaran Narayanasamy、Nathan A. Labenz、M. Christina White
    DOI:10.1021/ja0500198
    日期:2005.5.18
    We are reporting a mild, chemo-, and highly regioselective Pd(II)-catalyzed allylic oxidation of alpha-olefins to furnish branched allylic esters that proceeds via a novel serial ligand catalysis mechanism in which two different ligands (i.e., vinyl sulfoxide 2 and BQ) interact sequentially with the metal to promote distinct steps of the catalytic cycle (i.e., C-H cleavage and pi-allyl functionalization
    我们正在报告一种温和的、化学的和高度区域选择性的 Pd(II) 催化的 α-烯烃烯丙基氧化,以提供支链烯丙基酯,该反应通过一种新型的串联配体催化机制进行,其中两种不同的配体(即乙烯基亚砜 2 和BQ) 依次与金属相互作用以促进催化循环的不同步骤(即分别为 CH 裂解和 pi-烯丙基功能化)。
  • Absolute Rate Constants for α-Amide Radical Reactions
    作者:Osama M. Musa、Seung-Yong Choi、John H. Horner、Martin Newcomb
    DOI:10.1021/jo9717907
    日期:1998.2.1
    measured at ambient temperature. Radicals 4a and 4b were employed as radical clocks in indirect kinetic studies to determine rate constants for reaction of secondary alpha-amide radicals with Bu(3)SnH. The calibrated tin hydride trapping reaction was then employed to determine rate constants for cyclization of the 1-(diethylcarbamoyl)-5-hexenyl radical (12). The rate constants for 5-exo cyclizations of secondary
    1-(二乙基氨基甲酰基)-6,6-二苯基-5-己烯基(4a),1-(二乙基氨基甲酰基)-7,7-二苯基-6-庚烯基(4b)和1-(二乙基氨基甲酰基)-通过激光闪光光解法由相应的PTOC酯(羧酸和N-羟基吡啶-2-硫酮的酸酐)制得1-甲基-6,6-二苯基-5-己烯基(4c)。在各种温度下测量自由基4a和4b的环化动力学,并在环境温度下测量4c的环化动力学。自由基4a和4b在间接动力学研究中用作自由基钟,以确定仲α-酰胺自由基与Bu(3)SnH反应的速率常数。然后将校准的氢化锡捕获反应用于确定1-(二乙基氨基甲酰基)-5-己烯基(12)环化的速率常数。仲α-酰胺基的5-exo环化的速率常数与其同构烷基自由基类似物的速率常数相似。叔α-酰胺基团4c的5-exo环化和仲α-酰胺基团4b的6-exo环化的速率常数小于类似的烷基和α-酯取代的基团的速率常数效果。仲α-酰胺自由基的氢化锡捕获速率常数类似
  • Polar group-containing olefin copolymer, process for preparing the same, thermoplastic resin composition contaning the copolymer, and uses thereof
    申请人:MITSUI CHEMICALS, INC.
    公开号:EP1186619A2
    公开(公告)日:2002-03-13
    The present invention is intended to provide a polar group-containing olefin copolymer having excellent adhesion properties to metals or polar resins and excellent compatibility therewith, a process for preparing the copolymer, a thermoplastic resin composition containing the copolymer, and uses thereof. The polar group-containing olefin copolymer comprises a constituent unit derived from an α-olefin of 2 to 20 carbon atoms, and a constituent unit derived from a straight-chain, branched or cyclic polar group-containing monomer having at the end a polar group such as a hydroxyl group or an epoxy group and/or a constituent unit derived from a macromonomer having at the end a polymer segment obtained by anionic polymerization, ring-opening polymerization or polycondensation. The polar group-containing olefin copolymer can be prepared by polymerizing the α-olefin with the polar group-containing monomer and/or the macromonomer in the presence of a metallocene catalyst. The polar group-containing olefin copolymer and the thermoplastic resin composition containing the copolymer are used for films, sheets, modifiers, building/civil engineering materials, automobile exterior trim, electric/electronic parts, coating bases, compatibilizing agents, etc.
    本发明旨在提供一种对金属或极性树脂具有极佳粘附性和相容性的含极性基团的烯烃共聚物、制备该共聚物的工艺、含有该共聚物的热塑性树脂组合物及其用途。含极性基团的烯烃共聚物包括一个由 2 至 20 个碳原子的 α-烯烃衍生的组成单元和一个由直链、支链或环状含极性基团单体衍生的组成单元,直链、支链或环状含极性基团单体的末端具有极性基团,如羟基或环氧基,和/或一个由大单体衍生的组成单元,大单体的末端具有通过阴离子聚合、开环聚合或缩聚反应获得的聚合物段。含极性基团的烯烃共聚物可通过在茂金属催化剂存在下使α-烯烃与含极性基团的单体和/或大单体聚合来制备。含极性基团的烯烃共聚物和含有该共聚物的热塑性树脂组合物可用于薄膜、板材、改性剂、建筑/土木工程材料、汽车外饰、电气/电子零件、涂层基料、相容剂等。
  • Polar group-containing olefin copolymer, process for preparing the same, thermoplastic resin composition containing the copolymer, and uses thereof
    申请人:——
    公开号:US20020156207A1
    公开(公告)日:2002-10-24
    The present invention is intended to provide a polar group-containing olefin copolymer having excellent adhesion properties to metals or polar resins and excellent compatibility therewith, a process for preparing the copolymer, a thermoplastic resin composition containing the copolymer, and uses thereof. The polar group-containing olefin copolymer comprises a constituent unit derived from an &agr;-olefin of 2 to 20 carbon atoms, and a constituent unit derived from a straight-chain, branched or cyclic polar group-containing monomer having at the end a polar group such as a hydroxyl group or an epoxy group and/or a constituent unit derived from a macromonomer having at the end a polymer segment obtained by anionic polymerization, ring-opening polymerization or polycondensation. The polar group-containing olefin copolymer can be prepared by polymerizing the &agr;-olefin with the polar group-containing monomer and/or the macromonomer in the presence of a metallocene catalyst. The polar group-containing olefin copolymer and the thermoplastic resin composition containing the copolymer are used for films, sheets, modifiers, building/civil engineering materials, automobile exterior trim, electric/electronic parts, coating bases, compatibilizing agents, etc.
    本发明旨在提供一种对金属或极性树脂具有极佳粘附性能和极佳相容性的含极性基团的烯烃共聚物、制备该共聚物的工艺、含有该共聚物的热塑性树脂组合物及其用途。含极性基团的烯烃共聚物包括一个由 2 至 20 个碳原子的&agr;-烯烃衍生的组成单元,以及一个由直链、支链或环状含极性基团单体衍生的组成单元,该单体末端具有极性基团,如羟基或环氧基,和/或一个由大单体衍生的组成单元,该大单体末端具有通过阴离子聚合、开环聚合或缩聚反应获得的聚合物段。含极性基团的烯烃共聚物可通过在茂金属催化剂存在下,将&agr;-烯烃与含极性基团的单体和/或大单体进行聚合来制备。含极性基团的烯烃共聚物和含有该共聚物的热塑性树脂组合物可用于薄膜、板材、改性剂、建筑/土木工程材料、汽车外饰、电气/电子零件、涂层基料、相容剂等。
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