2-(furan-2-yl)-1,3-oxathiolane | 81932-19-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氧硫杂环戊烷
• 英文名称: 2-(furan-2-yl)-1,3-oxathiolane
• 英文别名: 2-furan-2-yl-[1,3]oxathiolane；2-(2-furyl)-1,3-oxathiolane；1,3-Oxathiolane, 2-(2-furanyl)-
• CAS: 81932-19-6
• 化学式: C₇H₈O₂S
• 分子量: 156.205
• InChiKey: UIUKWKHPHFBJPG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  47.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(furan-2-yl)-1,3-oxathiolane 在 水 作用下， 以 乙醇 为溶剂， 以93%的产率得到糠醛
  参考文献：
  名称：

  Iodine–alumina as an efficient and useful catalyst for the regeneration of carbonyl functionality from the corresponding 1,3-oxathiolanes and 1,3-dithiolanes in aqueous system

  摘要：

  A simple and useful method has been demonstrated for the deprotection of 1,3-oxathiolanes and 1,3-dithiolanes to the corresponding carbonyl compounds in excellent yield by employing catalytic amount (30 mol %) of iodine supported on neutral alumina in ethanol-water or water. The major advantages of this protocol are mild reaction conditions, less reaction time, easy to handle, high yields, inexpensive reagent and environmentally benign. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2010.03.084
• 作为产物：
  描述：

  糠醛 、 2-巯基乙醇 在 polystyrene-sulfonic acid resin-D₇₂ 作用下， 以 甲苯 为溶剂， 反应 5.0h， 以78%的产率得到2-(furan-2-yl)-1,3-oxathiolane
  参考文献：
  名称：

  醇和醛制备缩醛的新催化方法

  摘要：

  摘要 使用树脂-D72 催化剂在回流和水分离器条件下，用乙二醇、3-氯-1,2-丙二醇、1,2-丙二醇和1,2,3-丙三醇以高产率研究了醛的缩醛化反应。该反应简单、高效且具有化学选择性，并且不涉及任何其他添加剂。

  DOI：

  10.1080/00397910600616628

文献信息

• LiBF₄ Catalyzed Chemoselective Conversion of Aldehydes to 1,3-Oxathiolanes and 1,3-Dithianes
  作者：J. S. Yadav、B. V. S. Reddy、Sushil Kumar Pandey

  DOI：10.1055/s-2001-10780

  日期：——

  Lithium tetrafluoroborate is found to be an efficient catalyst for the chemoselective protection of both aromatic and aliphatic aldehydes as 1,3-oxathiolanes and 1,3-dithianes under mild reaction conditions. Due to the neutral reaction conditions, this method is compatible with acid sensitive substrates.

  四氟硼酸锂被发现是一种高效的催化剂，可以在温和的反应条件下对芳香醛和脂肪醛进行化学选择性保护，生成1,3-氧硫环烷和1,3-二硫烷。由于反应条件中性，这种方法与酸敏感底物相容。
• Selective desulfurization of 1,3-dithianes, -oxathiolanes and -thiazolidines by tributyltin hydride
  作者：K Schmidt、S O'Neal、T.C Chan、C.P Alexis、J.M Uribe、K Lossener、C.G Gutierrez

  DOI：10.1016/s0040-4039(00)70682-4

  日期：1989.1

  Selective desulfurization of 2-alkyl-1,3-dithianes, -oxathiolanes, or -thiazolidines 1 with one equivalent of tri-n-butyltin hydride yields acyclic compounds R1R2CHX(CH2)nSSnBu3 (X = S,O,NH; n= 2,3), (2) which can be destannylated to the corresponding mercaptans 3.

  用一当量的氢化三正丁基锡对2-烷基-1,3-二硫杂环丁烷，-氧杂硫杂环戊烷或-噻唑烷1进行选择性脱硫，得到无环化合物R 1 R 2 CHX（CH 2）n SSnBu 3（X = S， O，NH； n ＝ 2，3），（2），其可被脱甲锡化为相应的硫醇3。
• Eco-friendly and Highly Chemoselective 1,3-Oxathio- and 1,3-Dithioacetalization of Aldehydes Using Ionic Liquids
  作者：J. S. Yadav、B. V. S. Reddy、G. Kondaji

  DOI：10.1246/cl.2003.672

  日期：2003.8

  Room temperature ionic liquids have been employed for the first time as novel and recyclable reaction media for the chemoselective conversion of aldehydes into their corresponding 1,3-oxathio- and dithioacetal derivatives in excellent yields under mild and neutral conditions. A wide range of functional and protecting groups such as TBDMS, PMB, THP, MOM, benzyl, propargyl ethers, acetonides, carbamates and esters are survived under these reaction conditions. The recovered activated ionic liquids can be recycled for four to five subsequent runs with consistency in activity.

  室温离子液体首次被用作新型且可回收的反应介质，用于在温和中性条件下将醛选择性转化为相应的1,3-氧硫杂环和二硫杂环衍生物，产率极佳。在这些反应条件下，包括TBDMS、PMB、THP、MOM、苄基、炔丙基醚、乙缩醛、氨基甲酸酯和酯等多种功能性和保护性官能团都能稳定存在。回收的活性离子液体可循环用于后续四到五次反应，活性保持一致。
• Montmorillonite K-10 Clay as an Efficient Solid Catalyst for Chemoselective Protection of Carbonyl Compounds as Oxathiolanes with 2-Mercaptoethanol
  作者：Nabin C. Barua、Siddhartha Gogoi、Jagat C. Borah

  DOI：10.1055/s-2004-829054

  日期：——

  Montmorillonite K-10 clay has been found to be a mild and efficient solid catalyst for the protection of a variety of carbonyl compounds, such as oxathiolanes, with 2-mercaptoethanol in good to excellent yields. In addition, by using this catalyst, high chemoselective protection of aldehydes in presence of ketones has been achieved.

  蒙脱石 K-10 粘土已被发现是一种温和而有效的固体催化剂，用于保护各种羰基化合物，如氧硫杂环戊烷，与 2-巯基乙醇以良好到极好的收率。此外，通过使用这种催化剂，在酮的存在下实现了对醛的高化学选择性保护。
• Blue LED-Promoted Oxathiacetalization of Aldehydes and Ketones
  作者：You-Chen Liu、Daggula Mallikarjuna Reddy、Xin-An Chen、Yi-Chen Shieh、Chin-Fa Lee

  DOI：10.1002/ejoc.202000218

  日期：2020.5.10

  A visible‐light‐promoted oxathiacetalization of aldehydes and ketones with 2‐mercaptoethanol and 3‐mercaptopropan‐1‐ol in the presence of eosin Y as catalyst is described leading to the formation of 1,3‐oxathiolanes and 1,3‐oxathianes at ambient temperature and under metal‐free conditions. The solvent is playing vital role in the protection of carbonyl compounds with mercaptoalcohol.

  描述了在曙红Y的催化下，使用2-巯基乙醇和3-巯基丙烷-1-醇在可见光条件下促进醛和酮的乙二醛乙醛缩醛化反应，从而导致1,3-氧杂硫杂环戊烷和1,3-氧杂蒽环的形成环境温度和无金属条件下。溶剂在用巯基醇保护羰基化合物中起着至关重要的作用。