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S-phenyl (3r,5r,7r)-adamantane-1-carbothioate

中文名称
——
中文别名
——
英文名称
S-phenyl (3r,5r,7r)-adamantane-1-carbothioate
英文别名
Phenyl 1-adamantanecarbothioate;S-phenyl adamantane-1-carbothioate
S-phenyl (3r,5r,7r)-adamantane-1-carbothioate化学式
CAS
——
化学式
C17H20OS
mdl
——
分子量
272.411
InChiKey
YPOHFYZEXCWHRL-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):
    4.8
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    sodium benzenesulfonate 在 tetrabutylammonium tetrafluoroborate 、 三苯基膦 作用下, 以 乙腈 为溶剂, 反应 2.0h, 生成 S-phenyl (3r,5r,7r)-adamantane-1-carbothioate
    参考文献:
    名称:
    酰氯和亚磺酸的电化学还原交叉偶联合成硫酯
    摘要:
    C-S键的构建是合成化学、药物化学和材料化学中的一个重要过程。硫醇通常用作提供 S 源的起始材料。然而,它们难闻的气味和毒性促使我们寻找替代品。在这种情况下,我们使用电化学还原方法从亚磺酸中获得硫自由基。在一个简单的未分裂池中,各种酰氯和亚磺酸是相容的,以高达 95% 的产率生成 40 个所需硫酯的例子。初步机制研究表明,亚磺酸形成硫自由基物质是通过单个电子转移过程的多个步骤进行的。
    DOI:
    10.1039/d2gc02424a
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文献信息

  • Radical reaction of S-phenyl chlorothioformate with alkyl iodides: free radical-mediated carboxylation approach
    作者:Sunggak Kim
    DOI:10.1039/a800664d
    日期:——
    Free radical-mediated carboxylation is achieved by treatment of alkyl iodides with S-phenyl chlorothioformate and bis(tributyltin) with irradiation at 300 nm.
    通过在300 nm波长照射下,使用S-苯基氯硫代甲酸酯和双(三丁基锡)处理烷基碘化物,实现了自由基介导的羧化反应。
  • An Efficient Synthesis of Thioesters Via TFA-Catalyzed Reaction of Carboxylic Acid and Thiols: Remarkably Facile C–S Bond Formation
    作者:Adel S. El-Azab、Alaa A.-M. Abdel-Aziz
    DOI:10.1080/10426507.2012.664220
    日期:2012.9.1
    Abstract A general, facile, and efficient new synthetic path to thioesters was established by employing defined TFA-catalyzed reaction of carboxylic acid and thiol under mild conditions. The structure of the newly synthesized compounds was determined by infrared spectroscopy, nuclear magnetic resonance, and a single crystal X-ray crystallographic analysis. Supplemental materials are available for this
    摘要 通过在温和条件下采用特定的三氟乙酸催化羧酸和硫醇的反应,建立了一种通用、简便、高效的硫酯合成新途径。新合成化合物的结构通过红外光谱、核磁共振和单晶 X 射线晶体学分析确定。补充材料可用于本文。转至出版商在线版的磷、硫和硅及相关元素,查看免费的补充文件。图形概要
  • Photocatalytic Phosphine-Mediated Thioesterification of Carboxylic Acids with Disulfides
    作者:Junqi Su、Aobo Chen、Guofeng Zhang、Ziyu Jiang、Jiannan Zhao
    DOI:10.1021/acs.orglett.3c03249
    日期:2023.11.10
    Herein, a practical and effective synthesis of thioesters from readily available carboxylic acids and odorless disulfides was developed under photocatalytic conditions. This approach involves phosphoranyl radical-mediated fragmentation to generate acyl radicals and allows for incorporation of both S atoms of the disulfides into the desired products. In addition to batch reactions, a continuous-flow
    在此,在光催化条件下开发了一种实用且有效的由容易获得的羧酸和无味二硫化物合成硫酯的方法。该方法涉及正膦基自由基介导的断裂以产生酰基自由基,并允许将二硫化物的两个S原子掺入所需的产物中。除了间歇反应外,还采用了连续流反应器,能够实现克级的快速硫酯合成。还展示了初步实验机制研究和 dalcetrapib 的快速合成。
  • Synthesis of New 1-Adamantanecarboxylic Acid Derivatives
    作者:E. A. Dikusar1'、N. G. Kozlov、V. I. Potkin、A. P. Yuvchenko、N. V. Kovganko
    DOI:10.1023/b:rujo.0000034968.28257.e9
    日期:2004.3
    Reactions of 1-adamantanecarbonyl chloride with functionally substituted alcohols, phenols, amines, thiols, and ketone oximes gave hitherto unknown 1-adamantanecarboxylic acid esters, amides, and thio esters, including those containing a peroxide group.
  • Tin-Free Radical Carbonylation: Thiol Ester Synthesis Using Alkyl Allyl Sulfone Precursors, Phenyl Benzenethiosulfonate, and CO
    作者:Sangmo Kim、Sunggak Kim、Noboru Otsuka、Ilhyong Ryu
    DOI:10.1002/anie.200501606
    日期:2005.9.26
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同类化合物

硫基丙酸苯酯 硫代乙酸S-[4-[二(2-氯乙基)氨基]苯基]酯 硫代乙酸 S-(2-乙基苯基)酯 乙硫酸,[[(1,1-二甲基乙基)二甲基甲硅烷基]氧代]-,S-苯基酯 S1,S2-二(4-氯苯基)乙烷二(硫代ate) S-苯基硫代异丁酸酯 S-苯基3-羟基硫代丁酸酯 S-苯基2-氟硫代乙酸酯 S-硫代乙酸苯酯 S-氯乙酰基-P-巯基甲苯 S-丙酰基-p-疏基甲苯 S-[4-[2-[4-(2-苯乙炔基)苯基]乙炔基]苯基]硫代乙酸酯 S-(三氟乙酰基)-4-疏基甲苯 S-(4-甲基苯基)硫代乙酸酯 S,S′-[1,4-亚苯基二(2,1-乙炔二基-4,1-亚苯基)]双(硫代乙酸酯) O-乙基S-(4-甲基苯基)单硫代草酸酯 4-溴苯基硫代乙酸酯 4-(S-乙酰基硫代)苯甲醛 4,4-二甲基-1-氧代-1-(苯基硫基)-2-戊烷基乙酸酯 3-氧代-3-(4-甲氧基苯氧基)丙酸 2-甲基苯硫酚乙酸酯 1-乙酰巯基-4-碘苯 S-(2-methoxyphenyl) 4-cyclopropylidenebutanethioate phenyl 3-methyl-2-cyclohexene-1-carbothioate S-(2-fluorophenyl) 2-methylpropanethioate 2-isopropylidenedithiosuccinic acid di-S-(4-fluorophenyl) ester thioacetic acid S-(4-ethyl-phenyl ester) S-phenyl 2,3-dimethyl-2-butenethioate 3-phenylsulfanylcarbonyl-propionic acid ethyl ester S-phenyl (3r,5r,7r)-adamantane-1-carbothioate (E)-S-Phenyl 4,4-dimethylpent-2-enethioate S-phenyl 2-(2-methoxyphenyl)ethanethioate S-phenyl (2R,3R)-3-(tert-butyldimethylsiloxy)-2-methyl-3-phenylpropanethioate S-(4-fluorophenyl) thiopivalate S-phenyl 2-methylbutanethioate S-phenyl 3-(phenyl((trimethylsilyl)oxy)amino)-3-(thiophen-2-yl)propanethioate S-phenyl 3-(4-bromophenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-phenyl-3-(phenyl((triethylsilyl)oxy)amino)propanethioate S-phenyl 3-cyclohexyl-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-(((tert-butyldimethylsilyl)oxy)(phenyl)amino)-3-phenylpropanethioate S-phenyl 3-(4-methoxyphenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-(phenyl((trimethylsilyl)oxy)amino)-3-(p-tolyl)propanethioate S-phenyl 3-(4-fluorophenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-phenyl-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate (E)-S-phenyl 5-phenyl-3-(phenyl((trimethylsilyl)oxy)amino)pent-4-enethioate S-phenyl 3-hydroxy-3-(4-methoxyphenyl)propanethioate S-phenyl 2-methyl-3-oxobutanethioate S-phenyl O-acetyl(thioglycolate) 6-Nitro-9-oxodecansaeure-phenylthioester 2-isopropylidenedithiosuccinic acid di-S-p-tolyl ester