2-[(4-methylphenyl)sulfonyl]benzofuran

• 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-[(4-methylphenyl)sulfonyl]benzofuran
• 英文别名: 2-(4-Methylphenyl)sulfonyl-1-benzofuran
• 化学式: C₁₅H₁₂O₃S
• 分子量: 272.324
• InChiKey: WVRJGUPVHLBFFO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  55.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  反式-2-羟基肉桂酸 在 copper(II) choride dihydrate 、 silver trifluoroacetate 、 caesium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 51.0h， 生成 2-[(4-methylphenyl)sulfonyl]benzofuran
  参考文献：
  名称：

  Copper/Silver-Mediated Cascade Reactions for the Construction of 2-Sulfonylbenzo[b]furans from trans-2-Hydroxycinnamic Acids and Sodium Sulfinates

  摘要：

  Efficient construction of 2-sulfonylbenzo[b]furans is achieved from readily available trans-2-hydroxycinnamic acids and sodium sulfinates mediated by the CuCl2 center dot 2H(2)O/AgTFA system under mild conditions. This unprecedented synthetic protocol provides expedient access to a series of products in one step via a protodecarboxylation/C-S bond formation/C-O bond formation cascade.

  DOI：

  10.1021/jo4024478

文献信息

• Synthesis of Diaryl Sulfones at Room Temperature: Cu-Catalyzed Cross-Coupling of Arylsulfonyl Chlorides with Arylboronic Acids
  作者：Feng Hu、Xiangyang Lei

  DOI：10.1002/cctc.201500174

  日期：2015.5.18

  An efficient and convenient method for the synthesis of diaryl sulfones was developed through the Cu‐catalyzed cross‐couplings of arylsulfonyl chlorides and arylboronic acids at room temperature in open air. This method is characterized by the use of inexpensive and readily available catalyst and substrates, mild reaction conditions, wide functionality tolerance, short reaction times for most substrates

  通过在室温下露天进行铜催化的芳基磺酰氯和芳基硼酸的交叉偶联反应，开发了一种有效，方便的合成二芳基砜的方法。该方法的特征在于使用廉价且容易获得的催化剂和底物，温和的反应条件，宽泛的功能耐受性，大多数底​​物的反应时间短以及中等至良好的产率。
• Catalyst-free arylation of sulfonamides <i>via</i> visible light-mediated deamination
  作者：Yong Luo、Hao Ding、Jing-Song Zhen、Xian Du、Xiao-Hong Xu、Han Yuan、Yi-Hui Li、Wan-Ying Qi、Bing-Zhe Liu、Shi-Man Lu、Can Xue、Qiuping Ding

  DOI：10.1039/d1sc02266k

  日期：——

  A novel arylation of sulfonamides with boronic acids to afford numerous diaryl sulfones via a visible light-mediated N–S bond cleavage other than the typical transition-metal-catalyzed C(O)–N bond activation is described. This methodology, which represents the first catalyst-free protocol for the sulfonylation of boronic acids, is characterized by its simple reaction conditions, good functional group

  描述了磺酰胺与硼酸的新型芳基化反应，通过可见光介导的 N-S 键断裂，而不是典型的过渡金属催化的 C(O)-N 键活化，从而提供多种二芳基砜。该方法代表了硼酸磺酰化的第一个无催化剂方案，具有反应条件简单、官能团耐受性好和效率高的特点。多种磺胺类后期功能化的几个成功例子表明该方法在药物科学和有机合成中具有很高的潜在效用。
• Preparation of organostannanes by intermolecular radical substitution reactions
  作者：K. Aboutayab、S. Caddick、K. Jenkins、S. Joshi、S. Khan

  DOI：10.1016/0040-4020(96)00660-6

  日期：1996.8

  novel radical substitution reaction of aromatic sulfones is presented. Thus, α-heterocyclic aromatic sulphones derived from indole, pyrrole, pyrazole, furans and thiophenes undergo rapid and high yielding ipso-substitution to furnish organostannanes. This methodology has been extended to β-heterocyclic aromatic sulfones derived from indoline and dibenzofuran. The methodology has some liminations as

  提出了一种通过芳族砜的新型自由基取代反应合成芳族锡烷的新方法。因此，衍生自吲哚，吡咯，吡唑，呋喃和噻吩的α-杂环芳族砜经历快速且高产率的ipso取代以提供有机锡烷。该方法已经扩展到衍生自二氢吲哚和二苯并呋喃的β-杂环芳族砜。该方法有一些局限性，如3-苯基磺酰基吲哚衍生物17和某些苯硫基取代的杂芳族体系22-24缺乏反应性。苯亚磺酰基取代的吲哚也可以进行所需的取代反应，如成功转化25到对应的锡烷4a上。
• Photochemical Halogen-Bonding Promoted Synthesis of Vinyl Sulfones via Vinyl and Sulfonyl Radicals
  作者：Zhou Jiang、Ke You、Haibo Wu、Mengyu Xu、Tao Wang、Jin Luo

  DOI：10.1021/acs.orglett.3c03958

  日期：2024.1.26

  A photochemical halogen-bonding-assisted synthesis of vinyl sulfones via radical–radical cross-coupling of vinyl bromines and sodium sulfinates is developed. This methodology offers a facile and efficient approach to various vinyl sulfones with excellent functional group tolerance under metal-, photocatalyst-, base-, and oxidant-free conditions. The reaction is also applicable for the late-stage functionalization

  通过乙烯基溴和亚磺酸钠的自由基-自由基交叉偶联，开发了一种光化学卤素键辅助合成乙烯基砜的方法。该方法为各种乙烯基砜提供了一种简便有效的方法，在无金属、光催化剂、碱和氧化剂的条件下具有优异的官能团耐受性。该反应也适用于药物分子的后期功能化和百克规模。此外，代替制备亚硫酸钠，这些反应也可以使用磺酰氯以一锅法进行。
• <i>N</i>-Sulfonylbenzotriazoles as Advantageous Reagents for <i>C</i>-Sulfonylation
  作者：Alan R. Katritzky、Ashraf A. A. Abdel-Fattah、Anatoliy V. Vakulenko、Hui Tao

  DOI：10.1021/jo051157i

  日期：2005.11.1

  Reactions of readily available N-(alkyl-, aryl-, and heteroarylsulfonyl)benzotriazoles 3a-h with diverse nitriles, reactive heteroaromatics, alkylheteroaromatics, sulfones, and esters produced alpha-cyanoalkyl sulfones 5a-i, sulfonylheteroaromatics 7a-e, alpha-(sulfonylalkyl)heterocycles 9a-f, alpha-sulfonylalkyl sulfones 11a-g, and esters of alpha-sulfonyl acids 14a-c, respectively, in synthetically useful to excellent yields. The results represent the first examples of the successful application of sulfonylazoles for C-sulfonylation.