2-((3,4-dimethoxybenzyl)thio)benzo[d]thiazole | 321973-70-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-((3,4-dimethoxybenzyl)thio)benzo[d]thiazole
• 英文别名: 2-{[(3,4-Dimethoxyphenyl)methyl]sulfanyl}-1,3-benzothiazole；2-[(3,4-dimethoxyphenyl)methylsulfanyl]-1,3-benzothiazole
• CAS: 321973-70-0
• 化学式: C₁₆H₁₅NO₂S₂
• mdl: MFCD00720346
• 分子量: 317.433
• InChiKey: POJHJZHJCMZRCS-UHFFFAOYSA-N

物化性质

• 沸点：
  471.6±55.0 °C(Predicted)
• 密度：
  1.31±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  21
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  84.9
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  3,4-二甲氧基苄醇 在 樟脑醌 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 14.0h， 生成 2-((3,4-dimethoxybenzyl)thio)benzo[d]thiazole
  参考文献：
  名称：

  Camphorquinone: a new and efficient oxidant for the preparation of 2-thio-substituted benzothiazoles from alcohols by oxidation-reduction condensation

  摘要：

  A convenient one-pot procedure for the preparation of various 2-thio-substituted benzothiazoles from alcohols and benzothiazole-2-thiol utilizing camphorquinone-mediated oxidation-reduction condensation is disclosed. The condensation between benzothiazole-2-thiol and alkyl diphenylphosphinites, generated in situ from alcohols and chlorodiphenylphosphine, proceeded smoothly in the presence of camphorquinone to furnish the corresponding benzothiazoles in good to moderate yields.[GRAPHICS].

  DOI：

  10.1080/17415993.2014.907408

文献信息

• Efficient Thiolation of Alcohols Catalyzed by Long Chained Acid-Functionalized Ionic Liquids under Mild Conditions
  作者：Chengxia Miao、Hongfeng Zhuang、Yating Wen、Feng Han、Qing-Feng Yang、Lei Yang、Zhen Li、Chungu Xia

  DOI：10.1002/ejoc.201900169

  日期：2019.5.26

  Long chained and SO3H‐functionalized ionic liquids derived from pyrrolidine were employed as metal‐free, efficient and recyclable catalyst for thiolation of alcohols with several kinds of thiols, providing up to 99 % yield within 0.25 h at room temperature.

  吡咯烷衍生的长链SO 3 H官能化离子液体被用作无金属，高效且可回收的催化剂，用于醇与多种硫醇的硫醇化反应，在室温下0.25小时内提供高达99％的收率。
• Direct Synthesis of Thioethers from Carboxylates and Thiols Catalyzed by FeCl₃
  作者：Kunuru Venkatesham、Chitturi Bhujanga Rao、Chanti Babu Dokuburra、Richard A. Bunce、Yenamandra Venkateswarlu

  DOI：10.1021/acs.joc.5b02143

  日期：2015.11.20

  A new and efficient method has been developed for the synthesis of thioethers from carboxylates and thiols. The reaction proceeds via a Fe(III)-catalyzed direct displacement of carboxylates from benzylic or allylic esters by heterocyclic thiols. Short reaction times, good to excellent yields of products, and few side reactions are the significant features of the new protocol.

  已经开发了一种新的有效方法，用于从羧酸盐和硫醇合成硫醚。该反应通过杂环硫醇通过Fe（III）催化的羧酸酯从苄基或烯丙基酯直接置换而进行。新协议的显着特点是反应时间短，产品收率好至极好，副反应少。
• Acidic-functionalized ionic liquid as an efficient, green, and metal-free catalyst for benzylation of sulfur, nitrogen, and carbon nucleophiles to benzylic alcohols
  作者：Xue-Qiang Chu、Ran Jiang、Yi Fang、Zheng-Yang Gu、Hua Meng、Shun-Yi Wang、Shun-Jun Ji

  DOI：10.1016/j.tet.2012.11.045

  日期：2013.1

  A series of HSO4- functionalized ILs was synthesized and used as efficient, green, and metal-free catalysts for benzylation. Notably, the catalytic system has wide substrate scopes and the ionic liquid catalysts were applied to investigate three different types of nucleophiles to give the desired benzylation products with moderate to excellent yields. (C) 2012 Elsevier Ltd. All rights reserved.