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{2-(2-oxo-N-pyrrolidinyl)ethyl}diphenyltin iodide | 112714-53-1

中文名称
——
中文别名
——
英文名称
{2-(2-oxo-N-pyrrolidinyl)ethyl}diphenyltin iodide
英文别名
1-[2-[Iodo(diphenyl)stannyl]ethyl]pyrrolidin-2-one
{2-(2-oxo-N-pyrrolidinyl)ethyl}diphenyltin iodide化学式
CAS
112714-53-1
化学式
C18H20INOSn
mdl
——
分子量
511.977
InChiKey
KTIKMROBZLYGSJ-UHFFFAOYSA-M
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):
    2.8
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    {2-(2-oxo-N-pyrrolidinyl)ethyl}diphenyltin iodidesodium dimethyldithiocarbamate乙醇乙酸乙酯 为溶剂, 以81%的产率得到{2-(2-oxo-N-pyrrolidinyl)ethyl}(N,N-dimethyldithiocarbamato)diphenyltin
    参考文献:
    名称:
    [2-(2-吡啶基)乙基]-,[2-(4-吡啶基)乙基]-和[2-(2-氧代-N-吡咯烷基)乙基]三苯基锡(IV)的合成,表征和反应化学)
    摘要:
    The compounds Ph3SnR [R = (CH2)2C5H5N-2 (1), (CH2)2C5H5N-4 (2), and (CH2)2C3H6C(O)N-2 (3)] have been synthesized by hydrostannylation of 2- or 4-vinylpyridine and N-vinylpyrrolidin-2-one, respectively, with Ph3SnH. Reaction of 1-3 with 1 equiv of X2 (X = Br, I) gives Ph2RSnX, which have been used to synthesize representative compounds of general formula Ph2RSn(L), L = S2CNR'2 (R' = Me, Et) or O2CR' (R' = Me, Ph). The structures of the compounds are discussed on the basis of their H-1, C-13, Sn-119 NMR and Sn-119 Mossbauer data. The structure of Ph2Sn[(CH2)2C5H5N-2](S2CNMe2) has been determined by X-ray crystallography: C22H24N2S2Sn, fw 499.28, a = 9.611 (4) angstrom, b = 10.255 (3) angstrom, c = 12.896 (9) angstrom, a = 75.35 (4)-degrees, beta = 70.97 (4)-degrees, gamma = 68.09 (3)-degrees, V = 1102.2 angstrom3, Z = 2, space group P1BAR, rho(calc) = 1.50 g cm-3, mu(Mo Kalpha) = 12.42 cm-1, lambda(Mo Kalpha) = 0.710 69 angstrom, F(000) = 504, R = 0.0492, R(w) = 0.0542 for 2133 unique data. The tin is in a five-coordinate, trigonal bipyramidal trans-NSSnPh2R environment, with nitrogen and sulfur in the axial positions. The 2-ethylpyridyl ligand chelates the metal, while the dithiocarbamate is monodentate.
    DOI:
    10.1021/om00027a029
  • 作为产物:
    描述:
    {2-(2-oxo-N-pyrrolidinyl)ethyl}triphenyltin 在 I2 作用下, 以 氯仿 为溶剂, 以85%的产率得到{2-(2-oxo-N-pyrrolidinyl)ethyl}diphenyltin iodide
    参考文献:
    名称:
    [2-(2-吡啶基)乙基]-,[2-(4-吡啶基)乙基]-和[2-(2-氧代-N-吡咯烷基)乙基]三苯基锡(IV)的合成,表征和反应化学)
    摘要:
    The compounds Ph3SnR [R = (CH2)2C5H5N-2 (1), (CH2)2C5H5N-4 (2), and (CH2)2C3H6C(O)N-2 (3)] have been synthesized by hydrostannylation of 2- or 4-vinylpyridine and N-vinylpyrrolidin-2-one, respectively, with Ph3SnH. Reaction of 1-3 with 1 equiv of X2 (X = Br, I) gives Ph2RSnX, which have been used to synthesize representative compounds of general formula Ph2RSn(L), L = S2CNR'2 (R' = Me, Et) or O2CR' (R' = Me, Ph). The structures of the compounds are discussed on the basis of their H-1, C-13, Sn-119 NMR and Sn-119 Mossbauer data. The structure of Ph2Sn[(CH2)2C5H5N-2](S2CNMe2) has been determined by X-ray crystallography: C22H24N2S2Sn, fw 499.28, a = 9.611 (4) angstrom, b = 10.255 (3) angstrom, c = 12.896 (9) angstrom, a = 75.35 (4)-degrees, beta = 70.97 (4)-degrees, gamma = 68.09 (3)-degrees, V = 1102.2 angstrom3, Z = 2, space group P1BAR, rho(calc) = 1.50 g cm-3, mu(Mo Kalpha) = 12.42 cm-1, lambda(Mo Kalpha) = 0.710 69 angstrom, F(000) = 504, R = 0.0492, R(w) = 0.0542 for 2133 unique data. The tin is in a five-coordinate, trigonal bipyramidal trans-NSSnPh2R environment, with nitrogen and sulfur in the axial positions. The 2-ethylpyridyl ligand chelates the metal, while the dithiocarbamate is monodentate.
    DOI:
    10.1021/om00027a029
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文献信息

  • Synthesis, characterization, and reaction chemistry of [2-(2-pyridyl)ethyl]-, [2-(4-pyridyl)ethyl]-, and [2-(2-oxo-N-pyrrolidinyl)ethyl]triphenyltin(IV)
    作者:Mary F. Mahon、Kieran C. Molloy、Philip C. Waterfield
    DOI:10.1021/om00027a029
    日期:1993.3
    The compounds Ph3SnR [R = (CH2)2C5H5N-2 (1), (CH2)2C5H5N-4 (2), and (CH2)2C3H6C(O)N-2 (3)] have been synthesized by hydrostannylation of 2- or 4-vinylpyridine and N-vinylpyrrolidin-2-one, respectively, with Ph3SnH. Reaction of 1-3 with 1 equiv of X2 (X = Br, I) gives Ph2RSnX, which have been used to synthesize representative compounds of general formula Ph2RSn(L), L = S2CNR'2 (R' = Me, Et) or O2CR' (R' = Me, Ph). The structures of the compounds are discussed on the basis of their H-1, C-13, Sn-119 NMR and Sn-119 Mossbauer data. The structure of Ph2Sn[(CH2)2C5H5N-2](S2CNMe2) has been determined by X-ray crystallography: C22H24N2S2Sn, fw 499.28, a = 9.611 (4) angstrom, b = 10.255 (3) angstrom, c = 12.896 (9) angstrom, a = 75.35 (4)-degrees, beta = 70.97 (4)-degrees, gamma = 68.09 (3)-degrees, V = 1102.2 angstrom3, Z = 2, space group P1BAR, rho(calc) = 1.50 g cm-3, mu(Mo Kalpha) = 12.42 cm-1, lambda(Mo Kalpha) = 0.710 69 angstrom, F(000) = 504, R = 0.0492, R(w) = 0.0542 for 2133 unique data. The tin is in a five-coordinate, trigonal bipyramidal trans-NSSnPh2R environment, with nitrogen and sulfur in the axial positions. The 2-ethylpyridyl ligand chelates the metal, while the dithiocarbamate is monodentate.
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