3-羟基-4-甲基-2-苯基戊-1-烯 | 140226-81-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-羟基-4-甲基-2-苯基戊-1-烯
• 中文别名: 3-羟基-4-甲基-2-苯基戊-1-烯
• 英文名称: 3-Hydroxy-4-methyl-2-phenylpent-1-ene
• 英文别名: 2-phenyl-4-methylpent-1-en-3-ol；4-methyl-2-phenylpent-1-en-3-ol；1-Penten-3-ol, 4-methyl-2-phenyl-
• CAS: 140226-81-9
• 化学式: C₁₂H₁₆O
• 分子量: 176.258
• InChiKey: ZZCFIGMBVUUAOZ-UHFFFAOYSA-N

物化性质

• 沸点：
  275.3±9.0 °C(Predicted)
• 密度：
  0.962±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  3-羟基-4-甲基-2-苯基戊-1-烯 在 偶氮二异丁腈 、 三正丁基氢锡 、 sodium hydride 作用下， 以 苯 为溶剂， 反应 25.0h， 生成 isopropylisopropenylbenzene
  参考文献：
  名称：

  A convergent method for the stereoselective synthesis of trisubstituted alkenes

  摘要：

  A method for the stereoselective, convergent synthesis of trisubstituted alkenes has been developed. The procedure features the synthesis of allylic alcohols 9 by coupling an aldehyde with a vinyl organometallic reagent. Treatment of 9 with carbon disulfide and methyl iodide gave the intermediate allylic xanthates 10 that underwent facile [3,3]-sigmatropic rearrangement to give the dithiocarbonates 11 and 12, radical reduction of which gave the (E)-alkenes 13 as the major products.

  DOI：

  10.1021/jo00035a004
• 作为产物：
  描述：

  4-Methyl-2-phenylpent-1-en-3-one 在 sodium tetrahydroborate 、 cerium(III) chloride heptahydrate 作用下， 以 甲醇 为溶剂， 反应 0.25h， 生成 3-羟基-4-甲基-2-苯基戊-1-烯
  参考文献：
  名称：

  Nonenzymatic kinetic resolution of α-aryl substituted allylic alcohols catalyzed by acyl transfer catalyst Np-PIQ

  摘要：

  Chiral alpha-aryl substituted allylic alcohols are important versatile synthetic intermediates. We report here an effective nonenzymatic kinetic resolution of racemic alpha-aryl substituted allylic alcohols by introducing different aryl groups with acyl transfer catalyst Np-PIQ and propionic anhydride, providing moderate to good selectivity factors (S=12-37). (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2015.01.018

文献信息

• One-pot synthesis of α,β-epoxy ketones by palladium-catalyzed epoxidation–oxidation of terminal allylic alcohols
  作者：Fateh V. Singh、Jesus M. Pena、Hélio A. Stefani

  DOI：10.1016/j.tetlet.2010.01.065

  日期：2010.3

  herein is a one-pot synthesis of α,β-epoxy ketones using a palladium-catalyzed epoxidation–oxidation sequence. Functionalized terminal allylic alcohols are treated with m-CPBA under mild reaction conditions to obtain the α,β-epoxy ketones. The main benefit of this approach is that the epoxidation of the terminal double bond and the oxidation of the secondary alcohol occured in the same reaction under

  本文描述的是使用钯催化的环氧化-氧化顺序一锅法合成的α，β-环氧酮。官能终端烯丙基醇与处理米温和反应条件下-CPBA以获得α，β环氧酮。该方法的主要优点是，在温和的反应下，同一反应中发生了末端双键的环氧化和仲醇的氧化，并且在反应顺序中既允许了给电子功能，又吸收了吸电子功能。
• Aziridination of 2- and 3-phenyl-substituted allylic alcohols with 3-acetoxyaminoquinazolinones: probing the nature of the transition state from the diastereoselectivity of aziridination
  作者：Robert S. Atkinson、Sabri Ulukanli、Paul J. Williams

  DOI：10.1039/a902577d

  日期：——

  Aziridination of phenyl-substituted allylic alcohol 10 with 3-acetoxyaminoquinazolinone 3 (Q1NHOAc) and with 22 (Q2NHOAc) has been studied. The diastereoselectivity of these reactions is markedly changed by carrying them out in the presence of aqueous sodium hydrogen carbonate solution and under these conditions aziridinations of 10 and of its ester analogue 5 with Q2NHOAc give the same magnitude and

  已经研究了苯基取代的烯丙醇10与3-乙酰氧基氨基喹唑啉酮3（Q 1 NHOAc）和22（Q 2 NHOAc）的氮化。通过在碳酸氢钠水溶液中进行这些反应，可以显着改变这些反应的非对映选择性，并且在这些条件下，将10及其酯类似物5与Q 2 NHOAc进行叠氮化可以得到相同的幅度和非对映选择性（用Ph CO 2我）。非对映选择性的这些变化的解释是基于在存在和不存在乙酸的情况下，在用于10叠氮化的过渡态中氢键性质的差异。
• The kinetic resolution of allylic alcohols by a non-enzymatic acylation catalyst; application to natural product synthesis
  作者：Stéphane Bellemin-Laponnaz、Jennifer Tweddell、J. Craig Ruble、Frank M. Breitling、Gregory C. Fu

  DOI：10.1039/b002041i

  日期：——

  A planar-chiral DMAP derivative is shown to serve as an effective catalyst for the kinetic resolution of allylic alcohols; to illustrate its practical utility, the catalyst is applied to the resolution of two alcohols that have been employed as intermediates in recent natural product total syntheses.

  平面手性 DMAP 衍生物可作为烯丙醇动力学拆分的有效催化剂；为了说明其实际用途，该催化剂用于拆分两种醇，这些醇已在最近的天然产物全合成中用作中间体。
• Stereoselective Synthesis of cis-β-Methyl- and Phenyl-Substituted Alkenylboronates by Platinum-Catalyzed Dehydrogenative Borylation
  作者：Toshimichi Ohmura、Yuta Takasaki、Hideki Furukawa、Michinori Suginome

  DOI：10.1002/anie.200805406

  日期：2009.3.16

  Changing places: Intramolecular B(pin)/H exchange took place in the presence of a platinum–phosphane catalyst, giving synthetically useful cis‐β‐methyl‐substituted alkenylboronates stereoselectively (see scheme; B(pin)=4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolan‐2‐yl).

  变化的地方：分子内的B（pin）/ H交换是在铂-膦催化剂存在下进行的，立体选择性地合成了有用的顺式-β-甲基取代的烯基硼酸酯（参见方案； B（pin）= 4、4、5， 5-四甲基-1,3,2-二氧杂硼硼烷-2-基）。
• Synthesis of Functionalized Epoxides by Copper-Catalyzed Alkylative Epoxidation of Allylic Alcohols with Alkyl Nitriles
  作者：Ala Bunescu、Qian Wang、Jieping Zhu

  DOI：10.1021/acs.orglett.5b00571

  日期：2015.4.17

  A copper-catalyzed oxyalkylation of allylic alcohols using nonactivated alkyl nitriles as reaction partners was developed. A sequence involving generation of an alkyl nitrile radical followed by its addition to a double bond and a copper-mediated formation of C(sp3)–O bond was proposed to account for the reaction outcome. The protocol provided an efficient route to functionalized tri- and tetrasubstituted

  开发了使用未活化的烷基腈作为反应伙伴的铜催化的烯丙醇的烷氧基化反应。为了说明反应的结果，提出了一个序列，该序列涉及生成烷基腈自由基，然后将其添加至双键和铜介导的C（sp 3）-O键形成。该协议通过形成具有中等至极好非对映选择性的C（sp 3）–C（sp 3）和C（sp 3）–O键，为官能化的三取代和四取代的环氧化物提供了一条有效途径。