1-(hexa-1,2-dien-1-ylsulfonyl)-4-methylbenzene | 61783-80-0

• 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: 1-(hexa-1,2-dien-1-ylsulfonyl)-4-methylbenzene
• 英文别名: 1-Tosyl-1,2-hexadiene
• CAS: 61783-80-0
• 化学式: C₁₃H₁₆O₂S
• 分子量: 236.335
• InChiKey: DALUDJUHTISWDG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  42.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(hexa-1,2-dien-1-ylsulfonyl)-4-methylbenzene 在 四(三苯基膦)钯 、 溶剂黄146 作用下， 以 四氢呋喃 为溶剂， 反应 2.0h， 以45%的产率得到1-((1E,3E)-hexa-1,3-dien-1-ylsulfonyl)-4-methylbenzene
  参考文献：
  名称：

  1-和2-芳基磺酰基1,3-二烯的区域发散合成

  摘要：

  在通过使用π-烯丙基钯化学研究烯丙基砜的烷氧基化反应的过程中，我们发现了烯丙基砜的异构化为芳基磺酰基1，3-二烯。在酸例如乙酸的存在下，在钯催化的条件下，烯丙砜被转化为1-芳基磺酰基1，3-二烯。另一方面，在质子穿梭存在下使用三苯基膦的亲核催化产生2-芳基磺酰基1，3-二烯。因此，可以基于反应条件的变化随意制备芳基磺酰基二烯的任何一种区域异构体。

  DOI：

  10.1021/ol500259m
• 作为产物：
  描述：

  1-phenylseleno-2-(p-toluenesulfonyl)ethyne 在 间氯过氧苯甲酸 作用下， 以 氯仿 为溶剂， 反应 27.25h， 生成 1-(hexa-1,2-dien-1-ylsulfonyl)-4-methylbenzene
  参考文献：
  名称：

  Additions of Organocopper Reagents and Heteroatom Nucleophiles to 1-Phenylseleno-2-(p-toluenesulfonyl)ethyne. Preparation of Vinyl and Allenic Sulfones and Formation of Michael, Anti-Michael, and Rearrangement Products

  摘要：

  1-Phenylseleno-2-(p-toluenesulfonyl)ethyne (4) was produced nearly quantitatively from p-(toluenesulfonyl)ethyne and benzeneselenenyl chloride. It underwent stereo- and regioselective syn-additions of organocopper reagents RCu(CN)Li to the beta-position of the sulfone moiety to afford adducts 5. Further reaction of the products with reagents RCu(SePh)Li resulted in substitution of the phenylseleno group with retention of configuration. Control of E,Z-stereochemistry in the product beta,beta-disubstituted vinyl sulfones is therefore achieved by the order of addition of the reagents. Selenoxide syn-elimination of adducts 5 afforded the corresponding allenic sulfones. The additions of amines and alkoxides to 4 produced the corresponding anti-Michael regioisomers (where attack occurred a to the sulfone group) as the major or sole products. The additions were highly stereoselective, proceeding by anti-addition in the anti-Michael series and by syn-addition in the corresponding Michael regioisomers. The reactions of 4 with thiolates and selenolates were more complex, affording rearranged adducts and Michael adducts as the major and minor products, respectively. The formation of the rearranged products can be rationalized by a series of addition-elimination processes. Phenylselenoethyne (43) underwent conjugate additions of pyrrolidine, sodium methoxide, sodium ethanethiolate, and benzeneselenolate anion, affording the corresponding cis isomers via anti-addition. The experiments with heteroatom nucleophiles and acetylenes 4 and 43 show that the phenylseleno group has a surprisingly large activating effect upon conjugate additions.

  DOI：

  10.1021/jo981224r

文献信息

• Preparation of Propargylic Sulfinates and their [2,3]-Sigmatropic Rearrangement to Allenic Sulfones
  作者：Rama Rao Tata、Carissa S. Hampton、Michael Harmata

  DOI：10.1002/adsc.201600986

  日期：2017.4.3

  scope of the [2,3]‐sigmatropic rearrangement of propargylic sulfinates to allenic sulfones by silver catalysis was expanded. A series of new propargylic sulfinate esters was generated from a variety of aromatic and heteroaromatic sulfonyl chlorides and their rearrangement to allenic sulfones is reported. In addition, the synthesis of propargylic sulfinate esters containing electron‐withdrawing benzenesulfonyl

  通过银催化，炔丙基亚磺酸盐[2,3]-σ重排为烯丙基砜的范围扩大了。从各种芳族和杂芳族磺酰氯生成了一系列新的炔丙基亚磺酸酯，并报道了它们被重排为烯丙基砜。此外，据报道含有吸电子的苯磺酰氯的炔丙基亚磺酸酯的合成。
• 1-(Phenylseleno)-2-(p-toluenesulfonyl)ethyne. A Novel Acetylenic Sulfone That Undergoes Normal and Anti-Michael Nucleophilic Additions
  作者：T Back

  DOI：10.1016/00404-0399(50)09253-

  日期：1995.7.3
• Preparation of allenic sulfones and allenes from the selenosulfonation of acetylenes
  作者：Thomas G. Back、M. Vijaya Krishna、K. Raman Muralidharan

  DOI：10.1021/jo00278a030

  日期：1989.8
• Barbarella, Giovanna; Cinquini, Mauro; Colonna, Stefano, Journal of the Chemical Society. Perkin transactions I, 1980, p. 1646 - 1649
  作者：Barbarella, Giovanna、Cinquini, Mauro、Colonna, Stefano

  DOI：——

  日期：——
• Asymmetric selenoxide elimination leading to chiral allenic sulfones
  作者：Naoki Komatsu、Tatsushi Murakami、Yoshiaki Nishibayashi、Toshio Sugita、Sakae Uemura

  DOI：10.1021/jo00066a023

  日期：1993.7

  Asymmetric oxidation of some aryl vinyl selenides (3) with Sharpless (A-C), modified Sharpless (D) or David oxidants (E-G) resulted in the formation of chiral allenic sulfones 5 of up to 42% enantiomeric excess (ee) via double asymmetric induction, i.e., asymmetric oxidation to selenoxide followed by its asymmetric elimination. The nature of aryl group of the selenides 3 showed a remarkable effect upon the ee of the product: o-nitrophenyl group (a) gave the highest ee, followed by o,p-dinitrophenyl (b), o-(trifluoromethyl)phenyl (e), and o-methoxyphenyl (f) groups, while phenyl (e) and 2-pyridyl (d) groups were not effective at all. The effects of aryl groups were kinetically analyzed by comparing the rate constants of both steps (k1 for oxidation step and k2 for elimination step) which were determined by H-1-NMR analysis of the concentration of 3, the intermediate selenoxides 4, and 5. As a result, it was disclosed that the ratio of these rate constants (k1/k2) Was closely related to the ee of the product; the smaller the ratio is, the larger the ee becomes.