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PhSO2CH(Sn(n-Bu)3)CH2CH2OCPh3 | 1190600-29-3

中文名称
——
中文别名
——
英文名称
PhSO2CH(Sn(n-Bu)3)CH2CH2OCPh3
英文别名
——
PhSO2CH(Sn(n-Bu)3)CH2CH2OCPh3化学式
CAS
1190600-29-3
化学式
C40H52O3SSn
mdl
——
分子量
731.627
InChiKey
KIVCAGHNFRISEA-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):
    10.62
  • 重原子数:
    45
  • 可旋转键数:
    11
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    35.7
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    PhSO2CH2CH2CH2OCPh3 、 三丁基氯化锡正丁基锂 作用下, 以 正戊烷 为溶剂, 以42%的产率得到PhSO2CH(Sn(n-Bu)3)CH2CH2OCPh3
    参考文献:
    名称:
    Lithiated γ-O-functionalized propyl phenyl sulfides and sulfones of the type Li[CH(SOxPh)CH2CH2OR] (x=0, 2). [Li{CH(SPh)CH2CH2Ot-Bu}(tmeda)] – A structurally characterized organolithium inner complex
    摘要:
    Lithiation of O-functionalized alkyl phenyl sulfides PhSCH2CH2CH2OR (R = Me, 1a; i-Pr, 1b; t-Bu, 1c; CPh3, 1d) with n-BuLi/tmeda in n-pentane resulted in the formation of alpha-and ortho-lithiated compounds [Li{CH(SPh)CH2CH2OR}(tmeda)] (alpha-2a-d) and [Li{o-C6H4SCH2CH2CH2OR)(tmeda)] o-2a-d), respectively, which has been proved by subsequent reaction with n-Bu3SnCl yielding the requisite stannylated gamma-OR-functionalized propyl phenyl sulfides n-Bu3SnCH(SPh)CH2CH2OR (alpha-3a-d) and n-Bu3Sn(o-C6H4SCH2CH2CH2OR) (o-3a-d). The a/ortho ratios were found to be dependent on the sterical demand of the substituent R. Stannylated alkyl phenyl sulfides alpha-3a-c were found to react with n-BuLi/tmeda and n-BuLi yielding the pure a-lithiated compounds alpha-2a-c and [Li{CH(SPh)CH2CH2OR}] (alpha-4a-b), respectively, as white to yellowish powders. Single-crystal X-ray diffraction analysis of [Li{CH(SPh) CH(2)CH(2)Ot- Bu}(tmeda)] (alpha-2c) exhibited a distorted tetrahedral coordination of lithium having a chelating tmeda ligand and a C, O coordinated organyl ligand. Thus, alpha-2c is a typical organolithium inner complex. Lithiation of O-functionalized alkyl phenyl sulfones PhSO2CH2CH2CH2OR (R = Me, 5a; i-Pr, 5b; CPh3, 5c) with n-BuLi resulted in the exclusive formation of the a-lithiated products Li[CH(SO2Ph)CH2CH2OR] (6a-c) that were found to react with n-Bu3SnCl yielding the requisite alpha-stannylated compounds n-Bu3SnCH(SO2Ph) CH2CH2OR (7a-c). The identities of all lithium and tin compounds have been unambiguously proved by NMR spectroscopy (1H, 13C, 119Sn). (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2009.05.035
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文献信息

  • Lithiated γ-O-functionalized propyl phenyl sulfides and sulfones of the type Li[CH(SOxPh)CH2CH2OR] (x=0, 2). [Li{CH(SPh)CH2CH2Ot-Bu}(tmeda)] – A structurally characterized organolithium inner complex
    作者:Michael Block、Matthias Linnert、Santiago Gómez-Ruiz、Dirk Steinborn
    DOI:10.1016/j.jorganchem.2009.05.035
    日期:2009.9
    Lithiation of O-functionalized alkyl phenyl sulfides PhSCH2CH2CH2OR (R = Me, 1a; i-Pr, 1b; t-Bu, 1c; CPh3, 1d) with n-BuLi/tmeda in n-pentane resulted in the formation of alpha-and ortho-lithiated compounds [LiCH(SPh)CH2CH2OR}(tmeda)] (alpha-2a-d) and [Lio-C6H4SCH2CH2CH2OR)(tmeda)] o-2a-d), respectively, which has been proved by subsequent reaction with n-Bu3SnCl yielding the requisite stannylated gamma-OR-functionalized propyl phenyl sulfides n-Bu3SnCH(SPh)CH2CH2OR (alpha-3a-d) and n-Bu3Sn(o-C6H4SCH2CH2CH2OR) (o-3a-d). The a/ortho ratios were found to be dependent on the sterical demand of the substituent R. Stannylated alkyl phenyl sulfides alpha-3a-c were found to react with n-BuLi/tmeda and n-BuLi yielding the pure a-lithiated compounds alpha-2a-c and [LiCH(SPh)CH2CH2OR}] (alpha-4a-b), respectively, as white to yellowish powders. Single-crystal X-ray diffraction analysis of [LiCH(SPh) CH(2)CH(2)Ot- Bu}(tmeda)] (alpha-2c) exhibited a distorted tetrahedral coordination of lithium having a chelating tmeda ligand and a C, O coordinated organyl ligand. Thus, alpha-2c is a typical organolithium inner complex. Lithiation of O-functionalized alkyl phenyl sulfones PhSO2CH2CH2CH2OR (R = Me, 5a; i-Pr, 5b; CPh3, 5c) with n-BuLi resulted in the exclusive formation of the a-lithiated products Li[CH(SO2Ph)CH2CH2OR] (6a-c) that were found to react with n-Bu3SnCl yielding the requisite alpha-stannylated compounds n-Bu3SnCH(SO2Ph) CH2CH2OR (7a-c). The identities of all lithium and tin compounds have been unambiguously proved by NMR spectroscopy (1H, 13C, 119Sn). (C) 2009 Elsevier B.V. All rights reserved.
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