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4-decylsulfanylbutan-2-one | 93072-57-2

中文名称
——
中文别名
——
英文名称
4-decylsulfanylbutan-2-one
英文别名
4-(decylthio)butane-2-one;4-(decylthio)butan-2-one
4-decylsulfanylbutan-2-one化学式
CAS
93072-57-2
化学式
C14H28OS
mdl
——
分子量
244.442
InChiKey
MIUFKWCXLOAJQV-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:
    169-170 °C(Press: 3 Torr)
  • 密度:
    0.9034 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    4.84
  • 重原子数:
    16.0
  • 可旋转键数:
    12.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    17.07
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    4-decylsulfanylbutan-2-one甘油5-磺基水杨酸 作用下, 以 甲苯 为溶剂, 以51.2%的产率得到[2-(2-Decylsulfanyl-ethyl)-2-methyl-[1,3]dioxolan-4-yl]-methanol
    参考文献:
    名称:
    Sabirov, S. S.; Gnevasheva, L. M.; Ismailov, M. I., Journal of Organic Chemistry USSR (English Translation), 1984, vol. 20, p. 1239 - 1243
    摘要:
    DOI:
  • 作为产物:
    描述:
    S-decylisothiuronium bromidesodium hydroxide碳酸氢钠 作用下, 以 乙醇 为溶剂, 反应 1.67h, 生成 4-decylsulfanylbutan-2-one
    参考文献:
    名称:
    Sabirov, S. S.; Gnevasheva, L. M.; Ismailov, M. I., Journal of Organic Chemistry USSR (English Translation), 1984, vol. 20, p. 1239 - 1243
    摘要:
    DOI:
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文献信息

  • Dithiooxamide as an Effective Sulfur Surrogate for Odorless High-Yielding Carbon-Sulfur Bond Formation in Wet PEG200 as an Eco-Friendly, Safe, and Recoverable Solvent
    作者:Habib Firouzabadi、Nasser Iranpoor、Forough Gorginpour、Arash Samadi
    DOI:10.1002/ejoc.201500156
    日期:2015.5
    In this study, we have employed dithiooxamide, a solid, odorless, and commercially available compound, as a sulfur surrogate for the preparation of dialkyl sulfides from available alkyl halides in high yields. This sulfur transfer agent was also used for a copper-catalyzed high-yielding preparation of diaryl sulfides from their available aryl halides and for the preparation of thia-Michael adducts
    在这项研究中,我们使用二代草酰胺(一种固体、无味且可商购的化合物)作为代用品,以高产率从可用的卤代烷制备二烷基硫化物。这种转移剂还用于催化从可用的芳基卤化物制备二芳基硫化物的高产率,以及高产率制备杂-迈克尔加合物。所有反应均在无味条件下在湿 PEG200(PEG = 聚乙二醇)中进行,这是一种环保、安全且可回收的溶剂。这些协议很容易适用于大规模操作。
  • A facile generation of C–S bonds via one-pot, odourless and efficient thia-Michael addition reactions using alkyl, aryl or allyl halides, thiourea and electron-deficient alkenes in wet polyethylene glycol (PEG 200) under mild reaction conditions
    作者:Habib Firouzabadi、Nasser Iranpoor、Mohammad Abbasi
    DOI:10.1016/j.tet.2009.04.079
    日期:2009.7
    An efficient and odourless synthesis of thia-Michael adducts by the reaction of various organic halides (primary, secondary, tertiary, allylic, and benzylic), structurally diverse electron-deficient alkenes (ketones, esters, and acrylonitrile) and thiourea in the presence of sodium carbonate in wet polyethylene glycol (PEG 200) at 30–35 °C has been developed. This protocol is also a highly useful method
    通过在以下条件下,各种有机卤化物(伯,仲,叔,烯丙基和苄基),结构多样的电子缺陷烯烃(酮,酯和丙烯腈)和硫脲的反应,高效而无味地合成噻吩-迈克尔加合物在30–35°C的湿聚乙二醇(PEG 200)中开发了碳酸。该协议对于大规模操作也是非常有用的方法。
  • Pronounced Catalytic Effect of a Micellar Solution of Sodium Dodecyl Sulfate (SDS) on the Efficient C-S Bond Formation<i>via</i>an Odorless Thia-Michael Addition Reaction through the<i>in situ</i>Generation of<i>S</i>-Alkylisothiouronium Salts
    作者:Habib Firouzabadi、Nasser Iranpoor、Mohammad Abbasi
    DOI:10.1002/adsc.200800690
    日期:2009.3
    Abstractmagnified imageA pronounced catalytic effect of sodium dodecyl sulfate (SDS) was observed on thein situproduction ofS‐alkylisothiouronium saltsviathe reaction of primary, allyl and benzyl halides with thiourea in SDS droplets .Hydrolysis of the generatedS‐alkylisothiouronium salts in the palisade layer of the droplets produces the corresponding thiol moieties which are immediately added to the electron‐deficient olefins that are present in the micellar core to produce the thia‐Michael adducts. The entire route is an almost odorless process. The yields of the products are good to excellent and the method is applicable to large‐scale operation without any problem.
  • SABIROV, S. S.;GNEVASHEVA, L. M.;ISMAILOV, M. I.;ISOBAEV, M. D., ZH. ORGAN. XIMII, 1984, 20, N 7, 1362-1366
    作者:SABIROV, S. S.、GNEVASHEVA, L. M.、ISMAILOV, M. I.、ISOBAEV, M. D.
    DOI:——
    日期:——
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