3-Nitrophenylacyl-toluol-p-sulfonat | 92554-40-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3-Nitrophenylacyl-toluol-p-sulfonat
• 英文别名: 3-Nitro-ω-toluolsulfonyl-acetophenon, 3-Nitro-phenacyl-tosylat；α-tosyloxy-m-nitroacetophenone；m-nitro-α-tosyloxyacetophenone；Ethanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-(3-nitrophenyl)-；[2-(3-nitrophenyl)-2-oxoethyl] 4-methylbenzenesulfonate
• CAS: 92554-40-0
• 化学式: C₁₅H₁₃NO₆S
• 分子量: 335.337
• InChiKey: HBVCNBMWCAFKTA-UHFFFAOYSA-N

物化性质

• 熔点：
  129-130 °C
• 沸点：
  497.6±30.0 °C(Predicted)
• 密度：
  1.387±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  23
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  115
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  3-Nitrophenylacyl-toluol-p-sulfonat 以 水 、 二甲基亚砜 为溶剂， 反应 10.0h， 生成 2-羟基-1-(3-硝基苯基)-1-乙酮
  参考文献：
  名称：

  在无过渡金属的条件下由环己酮，α-羟基酮和苯胺区域选择性合成三组分1,2-二芳基吲哚†

  摘要：

  描述了一种在无过渡金属的条件下单罐合成1,2-二芳基吲哚的简便方法。环己酮通过脱氢芳构化过程用作芳基源。通过多米诺反应选择性地形成一个C–C和两个C–N键。该协议为从容易获得的环己酮，α-羟基酮和苯胺构建有价值的生物活性1,2-二芳基吲哚提供了便利的方法。

  DOI：

  10.1039/c9cc00943d
• 作为产物：
  描述：

  间硝基苯甲酸 在 乙酸酐 作用下， 生成 3-Nitrophenylacyl-toluol-p-sulfonat
  参考文献：
  名称：

  重氮烷与羧酸-二环己基碳二亚胺混合物的相互作用引起的重氮酮

  摘要：

  将羧酸（1摩尔）和二环己基碳二亚胺（1摩尔）在乙醚中的混合物加到重氮甲烷（1·25摩尔）或重氮乙烷（1·25摩尔）中，得到相应的重氮酮（（约0·5mol。）通过酸酐中间体。该方法对于制备重氮酮是有用的，重氮酮不能通过常规方法由酰氯制备。例如，制备3-氰基丙酰氯的尝试没有成功，但是将重氮甲烷添加到3-氰基丙酸和二环己基碳二亚胺的混合物中，在约1小时内得到4-重氮-3-氧代丁烷-1-腈。30％的产率。

  DOI：

  10.1039/j39700000971

文献信息

• Iodoarene-Mediated α-Tosyloxylation of Ketones with MCPBA and p-Toluenesulfonic Acid
  作者：Hideo Togo、Ayumi Tanaka、Katsuhiko Moriyama

  DOI：10.1055/s-0030-1260948

  日期：2011.8

  Alkyl aryl ketones and dialkyl ketones could be converted into the corresponding α-tosyloxy ketones by the reaction with MCPBA and p-toluenesulfonic acid monohydrate (PTSA˙H2O) in the presence of a catalytic amount of molecular iodine (I2) in a mixture of acetonitrile and 2,2,2-trifluoroethanol, although the yields were dependent on the ketones (method A). The same conversion of alkyl aryl ketones and dialkyl ketones into the corresponding α-­tosyloxy ketones could be smoothly carried out by the reaction with MCPBA and PTSA˙H2O in the presence of catalytic amounts of ­iodine and tert-butylbenzene in a mixture of acetonitrile and 2,2,2-trifluoroethanol (method B). In those reactions, p-iodotoluene and 4-tert-butyl-1-iodobenzene were formed at first in method A and method B, respectively, and then they were converted into p-[(hydroxy)(tosyloxy)]iodotoluene and 4-tert-butyl-1-[(hydroxy)(tosyloxy)iodo]benzene by the reaction with MCPBA and PTSA˙H2O. p-[(Hydroxy)(tosyloxy)]iodotoluene and 4-tert-butyl-1-[(hydroxy)-(tosyloxy)iodo]benzene worked as an α-tosyloxylation reagent of ketones.

  烷基芳基酮和二烷基酮可以通过与间氯过氧苯甲酸（MCPBA）和单水合对甲苯磺酸（PTSA·H2O）在催化量的碘分子（I2）存在下反应，在乙腈和2,2,2-三氟乙醇的混合物中，转化为相应的α-甲苯磺酰氧基酮，尽管产率取决于酮类（方法A）。烷基芳基酮和二烷基酮同样可以通过与MCPBA和PTSA· 在催化量的碘和叔丁基苯存在下反应，在乙腈和2,2,2-三氟乙醇的混合物中，顺利转化为相应的α-甲苯磺酰氧基酮（方法B）。在这些反应中，方法A和方法B分别首先形成对碘甲苯和4-叔丁基-1-碘苯，然后它们通过与MCPBA和PTSA· 反应转化为对[(羟基)(甲苯磺酰氧基)]碘甲苯和4-叔丁基-1-[(羟基)(甲苯磺酰氧基)碘]苯。对[(羟基)(甲苯磺酰氧基)]碘甲苯和4-叔丁基-1-[(羟基)(甲苯磺酰氧基)碘]苯作为酮的α-甲苯磺酰氧化试剂。
• 4-MeC6H4I-Mediated Efficient α-Tosyloxylation of Ketones with Oxone® and p-Toluenesulfonic Acid in Acetonitrile
  作者：Hideo Togo、Ayumi Tanaka

  DOI：10.1055/s-0029-1218370

  日期：2009.12

  Various alkyl aryl ketones, dialkyl ketones, and cycloheptanone were efficiently converted into the corresponding α-tosyl­oxy ketones in good yields by using Oxone® and p-toluenesulfonic acid monohydrate in the presence of p-iodotoluene in acetonitrile. 4-Methoxyacetophenone and 2-acetylthiophene bearing an electron-rich aromatic group could be also converted into the corresponding α-tosyloxyketones smoothly in good yields with the present method. Here, p-iodotoluene works as catalyst and p-[(hydroxy)(tosyloxy)]iodotoluene is formed in situ as a reactive species for the α-tosyloxylation of ketones. However, one equivalent of p-iodotoluene was required to obtain α-tosyloxyketones in good yields and was recovered in 80-20% yields, depending on the reaction conditions.

  通过在乙腈中使用Oxone®和p-甲苯磺酸一水合物，并在p-碘甲苯的存在下，各种烷基芳香酮、二烷基酮和环庚酮高效地转化为相应的α-甲苯磺酰氧基酮，产率良好。带有富电子芳香基团的4-甲氧基苯乙酮和2-乙酰基噻吩也可以用当前方法顺利地转化为相应的α-甲苯磺酰氧基酮，产率良好。在这里，p-碘甲苯作为催化剂，并且原位生成p-[(羟基)(甲苯磺酰氧基)]碘甲苯作为酮的α-甲苯磺酰氧化反应的活性物质。然而，为了获得良好的α-甲苯磺酰氧基酮产率，需要等量的p-碘甲苯，并且根据反应条件的不同，其回收率为80-20%。
• α-Tosyloxylation of ketones with ion-supported[hydroxy(tosyloxy)iodo] benzene
  作者：Feng Su、Jizhen Zhang、Guangyu Jin、Tao Qiu、Dejian Zhao、Hongbin Jia

  DOI：10.3184/030823409x12590815399135

  日期：2009.12

  room-temperature ionic liquid (RTIL) supported [hydroxy(tosyloxy)iodo]benzene (ion-supported HTIB) reagent was synthesised by three kinds of effective methods in high yields, which combined the advantages of ionic liquids and the hypervalent iodine. Ion-supported HTIB was an effective reagent for one-step conversion of ketones to the corresponding α-tosyloxylated ketones in the ionic liquid [emim]BF4or acetonitrile

  结合离子液体和高价碘的优点，采用三种有效的方法以高产率合成了一种新型的室温离子液体（RTIL）负载[羟基（甲苯磺酰氧基）碘]苯（离子负载HTIB）试剂。离子负载的 HTIB 是一种有效的试剂，用于在微波下将酮一步转化为离子液体 [emim]BF4 或乙腈中相应的 α-甲苯磺酰氧基化酮。转化反应后，试剂转化为离子负载的碘苯，易于回收和再生而不会损失活性。
• A Novel One-Pot Method for α-Tosyloxylation of Ketones Using a Catalytic Amount of Ammonium Iodide
  作者：Jie Yan、Jiantao Hu、Min Zhu、Yuan Xu

  DOI：10.1055/s-0031-1289750

  日期：2012.4

  A novel one-pot procedure was designed for the preparation of various α-tosyloxy ketones in good yields by the reaction of ketones with m-chloroperoxybenzoic acid and p-toluenesulfonic acid monohydrate in the presence of catalytic amounts of ammonium iodide and benzene in a mixture of acetonitrile and 2,2,2-trifluo­roethanol (8:2) at room temperature for 24 hours. α-tosyloxylation - α-tosyloxy ketones

  一种新的单罐方法被设计为通过与酮的反应制备以良好的收率各种α-甲苯磺酰氧基酮的米氯过氧酸和p -甲苯磺酸一水合物在催化量的碘化铵和苯的存在在混合物中在室温下将乙腈和2,2,2-三氟乙醇（8：2）混合24小时。 α-甲苯磺酰化-α-甲苯磺酰酮-高价碘中间体-碘化铵
• Effect of Substituents on the Regioselectivity of the Reaction of α-Tosyloxyketones with Thioureas in Acidic Medium: Access to 2-Aminothiazoles and 2-Imino-2,3-dihydrothiazoles
  作者：Ranjana Aggarwal、Rajiv Kumar、Dionisia Sanz、Rosa M. Claramunt

  DOI：10.1002/jhet.1676

  日期：2014.5

  Regioselective condensation of α‐tosyloxyacetophenones 1 and N‐substituted thioureas 2 in acidic medium to give regioisomers 2‐aminothiazoles I and 2‐imino‐2,3‐dihydrothiazoles II is largely influenced by the substituents present on 1 and 2. A mechanism, supported by DFT calculations has been proposed to explain the observed regioselectively.

  α-甲苯磺酰氧基苯乙酮1和N-取代的硫脲2在酸性介质中的区域选择性缩合反应产生区域异构体2-氨基噻唑I和2-亚氨基-2,3-二氢噻唑II在很大程度上受到1和2上存在的取代基的影响。已经提出了一种由DFT计算支持的机制来选择性地解释所观察到的区域。