3,3'-thiodiphenol | 63572-32-7

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 3,3'-thiodiphenol
• 英文别名: 3,3'-Sulfanediyldiphenol；3-(3-hydroxyphenyl)sulfanylphenol
• CAS: 63572-32-7
• 化学式: C₁₂H₁₀O₂S
• 分子量: 218.276
• InChiKey: GOWCECVOTUONTI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  65.8
• 氢给体数：
  2
• 氢受体数：
  3

安全信息

• 海关编码：
  2930909090

反应信息

• 作为反应物：
  描述：

  2-磺基苯甲酸酐 、 3,3'-thiodiphenol 在 对甲苯磺酸 作用下， 反应 9.0h， 以68%的产率得到o-(6-hydroxy-3-oxo-3H-thioxanthen-9-yl)benzenesulphonic acid
  参考文献：
  名称：

  Novel photosensitizers for the E/Z-isomerization of trienes. Part 1. Syntheses and application

  摘要：

  Uranine and its thioxanthene and selenoxanthene analogues, as well as the disodium salts of o-(6-hydroxy-3-oxo-3H-xanthen-9-yl)benzenesulphonic acid and its thioxanthene and selenoxanthene analogues, show different photosensitizer properties in the E/Z-isomerization of trienes. This has been verified by applying them to the technically useful conversion of tachysterol into previtamin D. The syntheses of the novel photosensitizers with thioxanthene and selenoxanthene moieties are also described.

  DOI：

  10.1039/p29910000523
• 作为产物：
  描述：

  3-碘苯酚 在 potassium thioacyanate 、 copper(II) oxide 、 potassium hydroxide 作用下， 以 二甲基亚砜 为溶剂， 反应 20.0h， 以75%的产率得到3,3'-thiodiphenol
  参考文献：
  名称：

  在无配体条件下纳米氧化铜催化对称二芳基硫化物的合成。

  摘要：

  在无配体条件下，由可回收氧化铜纳米粒子介导的 CS 交叉偶联反应中，硫氰酸钾充当有效的硫替代物。该协议避免了难闻的硫醇，用于合成各种对称的二芳基硫化物，通过不同的芳基卤化物与硫氰酸钾的交叉偶联，以中等至优异的产率提供相应的产品。

  DOI：

  10.3762/bjoc.7.101

文献信息

• Copper(II)-Catalyzed Single-Step Synthesis of Aryl Thiols from Aryl Halides and 1,2-Ethanedithiol
  作者：Yajun Liu、Jihye Kim、Heesun Seo、Sunghyouk Park、Junghyun Chae

  DOI：10.1002/adsc.201400941

  日期：2015.7.6

  single‐step synthesis of aryl thiols from aryl halides has been developed employing copper(II) catalyst and 1,2‐ethanedithiol. The key features are use of readily available reagents, a simple operation, and relatively mild reaction conditions. This new protocol shows a broad substrate scope with excellent functional group compatibility. A variety of aryl thiols are directly prepared from aryl halides in high

  利用铜（II）催化剂和1,2-乙二硫醇开发了一种高效的过渡金属催化的从芳基卤化物单步合成芳基硫醇的方法。关键特征是使用现成的试剂，简单的操作以及相对温和的反应条件。该新协议显示了广泛的底物范围，具有出色的官能团相容性。由芳基卤化物直接以高收率制备各种芳基硫醇。此外，芳基硫醇原位用于合成更高级的分子，例如二芳基硫醚和苯并噻吩。
• LiI/TBHP Mediated Oxidative Cross-Coupling of P(O)-H Compounds with Phenols and Various Nucleophiles: Direct Access to the Synthesis of Organophosphates
  作者：Thippani Anitha、Kashamalla Chinna Ashalu、Mummadi Sandeep、Aabid Mohd、Joanna Wencel-Delord、Francoise Colobert、Kallu Rajender Reddy

  DOI：10.1002/ejoc.201901362

  日期：2019.12.8

  Direct phosphorylation of P(O)–H compounds with various nucleophiles such as phenols, alcohols, amines and enols is described using oxidative cross‐coupling strategy. The phosphorylation of hydroxylated naphthyls and heteroarenes has been achieved. Main features of this transformation are short reaction time, functional group tolerance, and broad substrate scope.

  使用氧化交叉偶联策略描述了P（O）–H化合物与各种亲核试剂（例如苯酚，醇，胺和烯醇）的直接磷酸化作用。已经实现了羟基化的萘基和杂芳基的磷酸化。该转化的主要特征是反应时间短，官能团耐受性强和底物范围广。
• Efficient Copper(I)-Catalyzed S-Arylation of KSCN with Aryl Halides in PEG-400
  作者：Xiaokang Li、Tangjun Yuan、Junmin Chen

  DOI：10.1002/cjoc.201100209

  日期：2012.3

  A simple and efficient protocol for CuI‐catalyzed CS bond formation of aryl halides with KSCN to symmetrical diaryl sulfides was reported in PEG‐400 without any other additives. A variety of aryl halides were converted to the corresponding diaryl sulfides in good to excellent yields. The present procedure tolerated a variety of functional groups and the steric hindrance of ortho‐substituents on aryl

  一个简单的，高效的协议的CuI催化Ç  S键形成的芳基卤化物与KSCN到对称二芳基硫化物报道在PEG-400，没有任何其他添加剂。将各种芳基卤化物以良好或优异的产率转化为相应的二芳基硫醚。本方法可耐受多种功能基团，邻位取代基在芳基卤化物上的空间位阻不会影响结果。
• Copper oxide nanoparticles catalyzed synthesis of aryl sulfides via cascade reaction of aryl halides with thiourea
  作者：K. Harsha Vardhan Reddy、V. Prakash Reddy、J. Shankar、B. Madhav、B.S.P. Anil Kumar、Y.V.D. Nageswar

  DOI：10.1016/j.tetlet.2011.03.070

  日期：2011.5

  and highly efficient protocol for the synthesis of symmetrical aryl sulfides was developed by the cross-coupling of aromatic halides with inexpensive and commercially available thiourea which was used as an effective sulfur surrogate. The present cross-coupling protocol of thiourea, via cascade reaction with various substituted aryl halides, producing desired aryl sulfides, has an added advantage of

  通过芳族卤化物与廉价和可商购的硫脲的交叉偶联，开发出可循环的氧化铜纳米颗粒催化简单而高效的合成对称芳基硫醚的方法，该硫脲被用作有效的硫代用品。通过与各种取代的芳基卤化物的级联反应，产生所需的芳基硫醚，本发明的硫脲的交叉偶联方案具有避免臭味的硫醇的附加优点。
• ANALYTE DETECTION USING NEAR-INFRARED FLUOROPHORES
  申请人：Portland State University

  公开号：US20160223558A1

  公开（公告）日：2016-08-04

  Embodiments of compounds for selectively detecting an analyte are disclosed, along with methods and kits for detecting analytes with the compounds. The compounds are bridged viologen conjugates including at least one fluorophore according to the general structure At least one of R 1 /R 2 , R 2 /R 3 , R 3 /R 4 , R 5 /R 6 , R 6 /R 7 , and/or R 7 /R 8 together form a substituted or unsubstituted cycloalkyl or aryl.

  公开了用于选择性检测分析物的化合物实施例，以及使用这些化合物检测分析物的方法和试剂盒。这些化合物是包括至少一种荧光团的桥联紫罗兰类化合物，其一般结构如下：至少有R1/R2、R2/R3、R3/R4、R5/R6、R6/R7和/或R7/R8中的至少一对形成取代或未取代的环烷基或芳基。