N,N-diethyl-2-(toluene-4-sulfonyl)acetamide | 198077-47-3

• 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: N,N-diethyl-2-(toluene-4-sulfonyl)acetamide
• 英文别名: N,N-diethyl-2-(p-tosyl)acetamide；N,N-diethyl-2-tosylacetamide；N,N-diethyl-2-[(4-methylphenyl)sulfonyl]acetamide；N,N-diethyl-2-(4-methylphenyl)sulfonylacetamide
• CAS: 198077-47-3
• 化学式: C₁₃H₁₉NO₃S
• 分子量: 269.365
• InChiKey: OKRUMFNIMJUTAS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  62.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N,N-diethyl-2-(toluene-4-sulfonyl)acetamide 、 3-氯苄溴 在 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 反应 12.5h， 以79%的产率得到(E)-3-(3-chlorophenyl)-N,N-diethylacrylamide
  参考文献：
  名称：

  一种实用有效的合成（E）-β-芳基-α，β-不饱和酰胺的方法

  摘要：

  在本文中，我们报告了从α-磺酰基乙酰胺1和苄基溴衍生物2一步合成（E）-β-单取代的α，β-不饱和酰胺3的过程。

  DOI：

  10.1016/j.tet.2008.08.057
• 作为产物：
  描述：

  N,N-diethyl-2-[(4-methylphenyl)thio]acetamide 在 selenium(IV) oxide 、 双氧水 作用下， 以 甲醇 、 水 为溶剂， 反应 8.0h， 生成 N,N-diethyl-2-(toluene-4-sulfonyl)acetamide
  参考文献：
  名称：

  Spectroscopic and theoretical studies of some N,N-diethyl-2-[(4′-substituted)phenylsulfonyl]acetamides

  摘要：

  The analysis of the IR carbonyl band of the N,N-diethyl-2-[(4'-substituted)phenylsulfonyl]acetamides Et(2)NC(O)CH(2)S(O)(2)-C(6)H(4)-Y (Y = OMe 1, Me 2,1-13, Cl 4, Br 5, NO(2) 6) supported by B3LYP/6-31G(d,p) calculations for 3, indicated the existence of three pairs (anti and syn) of cis (c) and gauche (g(1) and g(2)) conformers in the gas phase, being the gauche conformers significantly more stable than the cis ones. The anti geometry is more stable than the syn one, for each pair of cis and gauche conformers. The summing up of the orbital (NBO analysis) and electrostatic interactions justifies quite well the populations and the v(CO) frequencies of the anti and syn pairs of c, g(1) and g(2) conformers. The IR higher carbonyl frequency component whose population is ca. 10%, in CCl(4), may be ascribed to the least stable and most polar cis conformer pair (in the gas phase) and the lower frequency component whose population is ca. 90%, to the summing up of the populations of the two most stable and least polar gauche conformer pairs (g(1) and g(2)) (in the gas phase). The reversal of the cis(c)/gauche (g(1) + g(2)) population ratio observed in chloroform ca. 60% (cis)/40% (gauche) and the occurrence of the most polar cis(c) conformer only, in acetonitrile, strongly suggests the coalescence of the two gauche components in a unique carbonyl band in solution. A further support to this rationalization is given by the single point PCM solvation model performed by HF/6-31G(d,p) method, which showed a progressive increase of the c/(g(1) + g(2)) ratio going from gas to CCl(4), to CHCl(3) and to CH(3)CN. X-ray single crystal analysis of 4 indicates that this compound assumes, in the solid state, the syn-clinal (gauche) conformation with respect to the [O=C-CH(2)-S] moiety, and the most stable anti geometry relative to the [C(O)N(CH(2)CH(3))(2)] fragment. In order to obtain larger energy gain from the crystal packing the molecules of 4 are linked in centrosymmetric dimers through two C-H center dot center dot center dot O interactions (C-H([O-Ph])center dot center dot center dot O([SO2])) forming a step ladder. (C) 2011 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.molstruc.2011.06.051

文献信息

• o-Iodoxybenzoic Acid (IBX)–Iodine Mediated One-Pot Deacylative Sulfonylation of 1,3-Dicarbonyl Compounds: A Synthesis of β-Carbonyl Sulfones
  作者：Chutima Kuhakarn、Praewpan Katrun、Teerawat Songsichan、Darunee Soorukram、Manat Pohmakotr、Vichai Reutrakul

  DOI：10.1055/s-0036-1588900

  日期：——

  combination of o-iodoxybenzoic acid (IBX) and a catalytic amount of iodine is found to promote a facile one-pot deacylative sulfonylation reaction of 1,3-dicarbonyl compounds with sodium sulfinates to yield β-carbonyl sulfones. The present method provides the target products bearing a wide variety of functional groups in one step and in good yields. A combination of o-iodoxybenzoic acid (IBX) and a catalytic

  摘要 发现邻碘氧苯甲酸（IBX）和催化量的碘的组合可促进1,3-二羰基化合物与亚磺酸钠的简便的一锅脱酰基磺酰化反应，生成β-羰基砜。本发明的方法一步一步提供高产率的带有多种官能团的目标产物。 发现邻碘氧苯甲酸（IBX）和催化量的碘的组合可促进1,3-二羰基化合物与亚磺酸钠的简便的一锅脱酰基磺酰化反应，生成β-羰基砜。本发明的方法一步一步提供高产率的带有多种官能团的目标产物。
• An efficient electrochemical synthesis of β-keto sulfones from sulfinates and 1,3-dicarbonyl compounds
  作者：Xiao-Jun Pan、Jian Gao、Gao-Qing Yuan

  DOI：10.1016/j.tet.2015.06.063

  日期：2015.8

  An efficient electrochemical synthesis of β-keto sulfones from sulfinates and 1,3-dicarbonyl compounds has been developed. The present electrochemical route could afford the target products in high to excellent yields under mild conditions.

  已经开发了由亚磺酸盐和1,3-二羰基化合物有效地电化学合成β-酮砜的方法。本发明的电化学途径可以在温和的条件下以高至优异的产率提供目标产物。
• Facile access to 3-sulfonylquinolines via Knoevenagel condensation/aza-Wittig reaction cascade involving <i>ortho</i>-azidobenzaldehydes and β-ketosulfonamides and sulfones
  作者：Ksenia Malkova、Andrey Bubyrev、Stanislav Kalinin、Dmitry Dar’in

  DOI：10.3762/bjoc.19.60

  日期：——

  Quinoline-based sulfonyl derivatives, and especially sulfonamides, are relevant and promising structures for drug design. We have developed a new convenient protocol for the synthesis of 3-sulfonyl-substituted quinolines (sulfonamides and sulfones). The approach is based on a Knoevenagel condensation/aza-Wittig reaction cascade involving o-azidobenzaldehydes and ketosulfonamides or ketosulfones as key building blocks. The protocol is appropriate for both ketosulfonyl reagents and α-sulfonyl-substituted alkyl acetates providing the target quinoline derivatives in good to excellent yields.

  喹啉基磺酰衍生物，尤其是磺酰胺类化合物，是药物设计中具有相关性和前景的结构。我们开发了一种新的简便方法来合成 3-磺酰基取代的喹啉类化合物（磺酰胺类和砜类）。该方法基于克诺文纳格尔缩合/扎-维蒂希级联反应，涉及邻氮代苯甲醛和酮基磺酰胺或酮基砜作为关键构筑基块。该方案既适用于酮磺酰试剂，也适用于 α-磺酰基取代的烷基乙酸酯，能以良好甚至优异的收率提供目标喹啉衍生物。
• A practical and efficient synthesis of (E)-β-aryl-α,β-unsaturated amides
  作者：Chih-Ching Chen、Jung-Chieh Ho、Nein-Chen Chang

  DOI：10.1016/j.tet.2008.08.057

  日期：2008.11

  In this paper, we report a one-step convergent synthesis of (E)-β-monosubstituted α,β-unsaturated amides 3 from α-sulfonyl acetamide 1 and benzyl bromide derivatives 2.

  在本文中，我们报告了从α-磺酰基乙酰胺1和苄基溴衍生物2一步合成（E）-β-单取代的α，β-不饱和酰胺3的过程。
• Spectroscopic and theoretical studies of some N,N-diethyl-2-[(4′-substituted)phenylsulfonyl]acetamides
  作者：Elisângela Vinhato、Paulo R. Olivato、Alessandro Rodrigues、Julio Zukerman-Schpector、Maurizio Dal Colle

  DOI：10.1016/j.molstruc.2011.06.051

  日期：2011.9

  The analysis of the IR carbonyl band of the N,N-diethyl-2-[(4'-substituted)phenylsulfonyl]acetamides Et(2)NC(O)CH(2)S(O)(2)-C(6)H(4)-Y (Y = OMe 1, Me 2,1-13, Cl 4, Br 5, NO(2) 6) supported by B3LYP/6-31G(d,p) calculations for 3, indicated the existence of three pairs (anti and syn) of cis (c) and gauche (g(1) and g(2)) conformers in the gas phase, being the gauche conformers significantly more stable than the cis ones. The anti geometry is more stable than the syn one, for each pair of cis and gauche conformers. The summing up of the orbital (NBO analysis) and electrostatic interactions justifies quite well the populations and the v(CO) frequencies of the anti and syn pairs of c, g(1) and g(2) conformers. The IR higher carbonyl frequency component whose population is ca. 10%, in CCl(4), may be ascribed to the least stable and most polar cis conformer pair (in the gas phase) and the lower frequency component whose population is ca. 90%, to the summing up of the populations of the two most stable and least polar gauche conformer pairs (g(1) and g(2)) (in the gas phase). The reversal of the cis(c)/gauche (g(1) + g(2)) population ratio observed in chloroform ca. 60% (cis)/40% (gauche) and the occurrence of the most polar cis(c) conformer only, in acetonitrile, strongly suggests the coalescence of the two gauche components in a unique carbonyl band in solution. A further support to this rationalization is given by the single point PCM solvation model performed by HF/6-31G(d,p) method, which showed a progressive increase of the c/(g(1) + g(2)) ratio going from gas to CCl(4), to CHCl(3) and to CH(3)CN. X-ray single crystal analysis of 4 indicates that this compound assumes, in the solid state, the syn-clinal (gauche) conformation with respect to the [O=C-CH(2)-S] moiety, and the most stable anti geometry relative to the [C(O)N(CH(2)CH(3))(2)] fragment. In order to obtain larger energy gain from the crystal packing the molecules of 4 are linked in centrosymmetric dimers through two C-H center dot center dot center dot O interactions (C-H([O-Ph])center dot center dot center dot O([SO2])) forming a step ladder. (C) 2011 Elsevier B.V. All rights reserved.