3-Phenyl-octan | 18335-15-4

• 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: 3-Phenyl-octan
• 英文别名: 3-phenyloctane；Octane, 3-phenyl-；octan-3-ylbenzene
• CAS: 18335-15-4
• 化学式: C₁₄H₂₂
• 分子量: 190.329
• InChiKey: XEYWPMIXBVMRLE-UHFFFAOYSA-N

物化性质

• 保留指数：
  1352;1355;1358;1366

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  14
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  3-Phenyl-octan 生成 (1-甲基庚基)苯.
  参考文献：
  名称：

  Nasterova, T. N.; Roshchupkina, I. Yu.; Pimerzin, A. A., Journal of applied chemistry of the USSR, 1988, vol. 61, # 7, p. 1445 - 1449

  摘要：

  DOI：
• 作为产物：
  描述：

  4-辛烷基苯 生成 3-Phenyl-octan
  参考文献：
  名称：

  Nasterova, T. N.; Roshchupkina, I. Yu.; Pimerzin, A. A., Journal of applied chemistry of the USSR, 1988, vol. 61, # 7, p. 1445 - 1449

  摘要：

  DOI：

文献信息

• Silica-Supported Heteropoly Acid Catalyst for Liquid-Phase Friedel–Crafts Reactions
  作者：Yusuke Izumi、Noriko Natsume、Harumi Takamine、Ikuyo Tamaoki、Kazuo Urabe

  DOI：10.1246/bcsj.62.2159

  日期：1989.7

  heteropoly acids such as 12-tungstophosphoric, molybdophosphoric, and tungstosilicic acids efficiently catalyzed Friedel–Crafts alkylation and acylation reactions of aromatic hydrocarbons with 1-octene, benzyl chloride and benzoyl chloride in the liquid phase. The catalytic activity of heteropoly acid was generally enhanced when supported on silica. Silica-supported tungstosilicic acid worked as an

  二氧化硅负载的Keggin型杂多酸，如12-磷钨酸、磷钼酸和钨硅酸，在液相中有效催化芳烃与1-辛烯、苄基氯和苯甲酰氯的Friedel-Crafts烷基化和酰化反应。当负载在二氧化硅上时，杂多酸的催化活性通常会增强。即使在对二甲苯与苯甲酰氯或苯甲酸酐的酰化反应中，二氧化硅负载的钨硅酸也作为不溶性多相催化剂起作用，尽管在重复使用过程中观察到失活。考虑到负载对甲苯磺酸是一种通常使用的典型强质子酸，其活性远不如负载杂多酸，
• Adsorption and catalytic properties of sulfated aluminum oxide modified with cobalt ions
  作者：S. N. Lanin、A. A. Bannykh、E. V. Vlasenko、I. N. Krotova、O. N. Obrezkov、M. I. Shilina

  DOI：10.1134/s0036024417010150

  日期：2017.1

  The adsorption properties of sulfated aluminum oxide (9% SO 2-4 /γ-Al2O3) and a cobalt-containing composite (0.5%Сo/SO 2-4 /γ-Al2O3) based on it are studied via dynamic sorption. The adsorption isotherms of such test adsorbates as n-hydrocarbons (C6–C8), benzene, ethylbenzene, chloroform, and diethyl ether are measured, and their isosteric heats of adsorption are calculated. It is shown that the surface

  硫酸化氧化铝的吸附性能（9％SO 2- 4 /γ-Al系2 ö 3）和含钴复合（0.5％Сo/ SO 2- 4 /γ-Al系2 ö 3）的基础上它进行了研究通过动态吸附。测量这些测试吸附物的吸附等温线，如正烃（C 6 –C 8），苯，乙苯，氯仿和二乙醚，并计算其等规吸附热。结果表明，三氧化二铝的表面基本上硫酸化提高了其电子接受性，所以SO的催化活性2- 4 /γ-Al系2 ö 3 在25–120°C的温度下，苯与辛烯1的液相烷基化反应比最初的氧化铝要高一个数量级。可以确定的是，用钴离子对硫酸氧化铝进行了其他改性，从而使该催化剂的活性提高了2-4倍。结果表明，能够强特异性吸附的吸附部位与两个捐赠（芳族化合物，二乙醚化学吸附）和接受硫酸化的γ-Al表面上的分子（氯仿）形式2 ö 3通过钴盐促进。
• Detailed Characterization of <i>p</i>-Toluenesulfonic Acid Monohydrate as a Convenient, Recoverable, Safe, and Selective Catalyst for Alkylation of the Aromatic Nucleus
  作者：Mathew P. D. Mahindaratne、Kandatege Wimalasena

  DOI：10.1021/jo971832r

  日期：1998.5.1

  Alkylation of the aromatic nucleus, an important reaction in industry and synthetic organic chemistry, has traditionally been carried out by the well-known Friedel-Crafts reaction employing Lewis acid catalysts such as AlCl3 and BF3 or by using highly reactive organometallic reagents. Although protic acids such as anhydrous HF and concentrated H2SO4 have also been used in the alkylation of the aromatic nucleus, the notoriously corrosive, highly toxic, and hazardous nature of these agents has precluded their common use under ordinary laboratory conditions. Various organic sulfonic acids have, on occasion, been used as catalysts in Friedel-Crafts alkylations, but to our knowledge the chemistry and the scope of these reactions for common laboratory use have never been exploited in detail. In the present study we have characterized commercially available p-toluenesulfonic acid monohydrate (TsOH) as an efficient catalyst for the intermolecular coupling of the aromatic nucleus with activated alkyl halides, alkenes, or tosylates under mild conditions in an open atmosphere. In comparison to conventional Friedel-Crafts catalysts such as AlCl3, BF3, HF, and concentrated H2SO4, the extent of the formation of undesired products from side reactions such as transalkylation, polymerization, etc. was minimal with the TsOH-catalyzed reaction. The ability to recover and reuse the catalyst from the reaction mixtures, minimal generation of environmentally unfriendly waste, high specificity of the reaction, and the low cost of the catalyst are important advantages of the TsOH catalyst over the other conventional Friedel-Crafts catalysts.
• Selective hydrogenation of substituted dienes catalyzed by an organoyttrium complex
  作者：Gary A. Molander、John O. Hoberg

  DOI：10.1021/jo00038a004

  日期：1992.6

  Cp*2YMe(THF) has been developed as an efficient catalyst for the selective reduction of substituted dienes.
• Olson, Industrial and Engineering Chemistry, 1960, vol. 52, p. 835
  作者：Olson

  DOI：——

  日期：——

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