3-(octylthio)propanenitrile | 35652-59-6

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 3-(octylthio)propanenitrile
• 英文别名: 3-(octylsulfanyl)propionitrile；3-octylsulfanylpropanenitrile
• CAS: 35652-59-6
• 化学式: C₁₁H₂₁NS
• 分子量: 199.36
• InChiKey: JBJSMCQYMGAWDZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  13
• 可旋转键数：
  9
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  49.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-(octylthio)propanenitrile 在 乙酰氯 作用下， 以 正己烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 45.5h， 生成
  参考文献：
  名称：

  Synthesis and properties of cross-linkable DNA duplex using 4-amino-2-oxo-6-vinyl-1,3,5-triazine

  摘要：

  We synthesized the DNA oligonucleotide containing a new cross-linkable 4-amino-2-oxo-6-vinyltriazine (AOVT) nucleobase analogue (Et-AOVT) and evaluated these properties. Our results of the cross-link assay and thermal denaturing assay of duplexes containing AOVT demonstrated that the additional aza of AOVT has an impact on the duplex stability and crosslink properties. Our data suggests that the additional 5-aza of AOVT is involved in the hydrogen bonding with the complementary guanine, and this hydrogen bonding system successfully flipped the reactive vinyl group out to the major groove of the duplex demonstrating a new paradigm of a "cross-linkable duplex". (C) 2017 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tet.2017.01.043
• 作为产物：
  描述：

  1-辛硫醇 、 丙烯腈 在 乙酸–三乙胺 作用下， 反应 0.02h， 以99%的产率得到3-(octylthio)propanenitrile
  参考文献：
  名称：

  醋酸 三乙铵（ TEAA）：一种可回收的廉价离子液体，可促进化学选择性的氮杂和 硫杂 迈克尔 反应

  摘要：

  用于化学选择性氮杂/硫杂一种新的，高效率的，廉价的，可回收，轻度，方便，和绿色协议 迈克尔 的胺/硫醇到α，β加成反应 - 使用三乙基乙酸铵（不饱和化合物 TEAA ）离子液体被开发。该催化剂可以循环使用十次，从而消除了对有毒和昂贵催化剂的需求。

  DOI：

  10.1007/s00706-008-0886-4

文献信息

• A facile generation of C–S bonds via one-pot, odourless and efficient thia-Michael addition reactions using alkyl, aryl or allyl halides, thiourea and electron-deficient alkenes in wet polyethylene glycol (PEG 200) under mild reaction conditions
  作者：Habib Firouzabadi、Nasser Iranpoor、Mohammad Abbasi

  DOI：10.1016/j.tet.2009.04.079

  日期：2009.7

  An efficient and odourless synthesis of thia-Michael adducts by the reaction of various organic halides (primary, secondary, tertiary, allylic, and benzylic), structurally diverse electron-deficient alkenes (ketones, esters, and acrylonitrile) and thiourea in the presence of sodium carbonate in wet polyethylene glycol (PEG 200) at 30–35 °C has been developed. This protocol is also a highly useful method

  通过在以下条件下，各种有机卤化物（伯，仲，叔，烯丙基和苄基），结构多样的电子缺陷烯烃（酮，酯和丙烯腈）和硫脲的反应，高效而无味地合成噻吩-迈克尔加合物在30–35°C的湿聚乙二醇（PEG 200）中开发了碳酸钠。该协议对于大规模操作也是非常有用的方法。
• Novel Synthesis of Methyl Ketones Based on the Blaise Reaction
  作者：H. Surya Prakash Rao、K. Padmavathy、K. Vasantham、Shaik Rafi

  DOI：10.1080/00397910802594276

  日期：2009.4.22

  Abstract A facile two-step synthesis of methyl ketones from alkyl nitriles via the Blaise conversion of nitriles into β-keto esters and acid-mediated hydrolysis followed by decarboxylation of the resulting β-keto esters is described.

  摘要描述了通过将腈转化为 β-酮酯和酸介导的水解，然后将所得 β-酮酯脱羧，从烷基腈轻松两步合成甲基酮。
• Molecular interactions between carbon nanotubes and ammonium ionic liquids and their catalysis properties
  作者：Pankaj Attri、Rohit Bhatia、Bharti Arora、Naresh Kumar、Ji Hoon Park、Ku Youn Baik、Geon Joon Lee、In Tae Kim、Je Huan Koo、Eun Ha Choi

  DOI：10.1016/j.materresbull.2014.03.025

  日期：2014.10
• Pronounced Catalytic Effect of a Micellar Solution of Sodium Dodecyl Sulfate (SDS) on the Efficient C-S Bond Formation<i>via</i>an Odorless Thia-Michael Addition Reaction through the<i>in situ</i>Generation of<i>S</i>-Alkylisothiouronium Salts
  作者：Habib Firouzabadi、Nasser Iranpoor、Mohammad Abbasi

  DOI：10.1002/adsc.200800690

  日期：2009.3

  Abstractmagnified imageA pronounced catalytic effect of sodium dodecyl sulfate (SDS) was observed on thein situproduction ofS‐alkylisothiouronium saltsviathe reaction of primary, allyl and benzyl halides with thiourea in SDS droplets .Hydrolysis of the generatedS‐alkylisothiouronium salts in the palisade layer of the droplets produces the corresponding thiol moieties which are immediately added to the electron‐deficient olefins that are present in the micellar core to produce the thia‐Michael adducts. The entire route is an almost odorless process. The yields of the products are good to excellent and the method is applicable to large‐scale operation without any problem.
• Triethylammonium acetate (TEAA): a recyclable inexpensive ionic liquid promotes the chemoselective aza- and thia-Michael reactions
  作者：Akhilesh K. Verma、Pankaj Attri、Varun Chopra、Rakesh K. Tiwari、Ramesh Chandra

  DOI：10.1007/s00706-008-0886-4

  日期：2008.9

  A new, highly efficient, inexpensive, recyclable, mild, convenient, and green protocol for chemoselective aza/thia- Michael addition reactions of amines/thiols to α,β - unsaturated compounds using triethylammonium acetate ( TEAA ) ionic liquid was developed. The catalyst can be recycled ten times and obviate the need for toxic and expensive catalysts.

  用于化学选择性氮杂/硫杂一种新的，高效率的，廉价的，可回收，轻度，方便，和绿色协议 迈克尔 的胺/硫醇到α，β加成反应 - 使用三乙基乙酸铵（不饱和化合物 TEAA ）离子液体被开发。该催化剂可以循环使用十次，从而消除了对有毒和昂贵催化剂的需求。