CAS: 928-92-7; (E)-Hex-4-En-1-Ol

该化合物是分子式C6H12O的不饱和脂性酒精,在4位置上具有一个反形的双联结,该化合物因其作为有机合成的中间体的作用而受到重视,特别是在香味,口味和特殊化学品的生产方面.其终端氢氧化物组和相混合的双联体使它成为进一步功能化,包括氧化,酯化或聚合的多功能性构件.(4E)异构体与其(4Z)对角相比,具有不同的再活动性,往往在某些合成途径中产生更高的选择性.其明确的液体形式和适度的挥发性有利于实验室和工业应用的处理.

结构式图片

相似化合物

35194-36-6 57074-37-0 764-37-4

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上下游产品

CAS号34495-74-4 (E)-hex-4-enoic... | CAS号821-41-0 5-己烯-1-醇 | CAS号928-93-8 己-4-炔-1-醇 | CAS号25166-87-4 反-4-己烯醛 | CAS号55230-25-6 5,6-Dihydro-2-m... | CAS号75-21-8 环氧乙烷 | CAS号4784-77-4 1-溴-2-丁烯 | CAS号60653-70-5 trans-hex-4-eny... | CAS号1003-30-1 2-Ethyltetrahyd... | CAS号10141-72-7 2-甲基四氢吡喃 | CAS号105679-06-9 2-(1-methylsulf... | CAS号85213-22-5 2-乙酰基-1-吡咯啉 | CAS号156051-16-0 3-溴-2-甲基四氢-2H-吡喃 | CAS号1003-28-7 2-乙基吡咯烷 | CAS号32821-68-4 3-乙基四氢-2H-吡喃-2-酮 | CAS号31502-25-7 6-bromohex-2-ene | CAS号134777-60-9 6-methoxyhex-2-ene

合成工艺路线路线简述

  • 合成目标产物 (E)-4-Hexen-1-Ol 主要起始原料 5-Hexen-1-Ol
  • 821-41-0 = 928-92-7
    反应条件:1.1 Reagents: (Ethenyloxy)Trimethylsilane Catalysts: (Sp-5-41)-Dichloro[1,3-Dihydro-1,3-Bis(2,4,6-Trimethylphenyl)-2H-Imidazol-2-Ylid... Solvents: Dichloromethane; 3 H,50 °C
    标题:Selective Isomerization Of A Terminal Olefin Catalyzed By A Ruthenium Complex: The Synthesis Of Indoles Through Ring-Closing Metathesis
    作者:Arisawa,Mitsuhiro; Terada,Yukiyoshi; Nakagawa,Masako; Nishida,Atsushi
    参考文献:Angewandte Chemie 日期:2002 卷标:41(24) 页码:4732-4734]

    34495-74-4 = 928-92-7
    反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether; 0 °C; 0 °C -> Rt; 3 H,Rt1.2 Reagents: Water1.3 Reagents: Sodium Hydroxide Solvents: Water
    标题:Total Synthesis Of (-)-Histrionicotoxin
    作者:Adachi,Yohei; Kamei,Noriyuki; Yokoshima,Satoshi; Fukuyama,Tohru
    参考文献:Organic Letters 日期:2011 卷标:13(16) 页码:4446-4449]

    34495-74-4 = 928-92-7
    反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether; 0 °C; 90 Min,0 °C1.2 Solvents: Ethyl Acetate1.3 Reagents: Water1.4 Reagents: Sodium Hydroxide Solvents: Water
    标题:Capturing Primary Ozonides For A Syn-Dihydroxylation Of Olefins
    作者:Arriaga,Danniel K.; Thomas,Andy A.
    参考文献:Nature Chemistry 日期:2023 卷标:15(9) 页码:1262-1266]

    55230-25-6 = 928-92-7
    反应条件:1.1 Reagents: Sodium Solvents: Ammonia
    标题:Stereoselective Synthesis Of Alkenyl Alcohols Using Dissolving Metal (Calcium,Sodium) Reduction
    作者:Zhou,Jingyao; Lu,Guodi; Huang,Xin; Wu,Shihui
    参考文献:Synthetic Communications 日期:1991 卷标:21(3) 页码:435-41]

    72081-15-3 = 928-92-7
    反应条件:1.1 Reagents: Methyllithium Catalysts: Cuprous Cyanide Solvents: Diethyl Ether,Pentane1.2 Reagents: Water
    标题:A Stereoselective Synthesis Of Functionalized Alkenyllithiums And Alkenyl Cyanocuprates By The Copper(I)-Catalyzed Coupling Of Organolithium Reagents With α-Lithiated Cyclic Enol Ethers
    作者:Kocienski,Philip; Wadman,Sjoerd; Cooper,Kelvin
    参考文献:Journal Of The American Chemical Society 日期:1989 卷标:111(6) 页码:2363-5]

    31535-05-4 = 928-92-7
    反应条件:1.1 Reagents: Sodium
    标题:3,4-Dihydro-2H-Pyran
    作者:Kierkus,Paul Ch.
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2001 卷标:1 页码:1-4]

    2430-27-5 = 928-92-7
    反应条件:1.1 Reagents: Sodium Bicarbonate,Oxygen Solvents: Acetone,Ethyl Acetate; 40 Min,Rt; 1 H
    标题:Characterization Of An Epoxide Hydrolase From The Florida Red Tide Dinoflagellate,Karenia Brevis
    作者:Sun,Pengfei; Leeson,Cristian; Zhi,Xiaoduo; Leng,Fenfei; Pierce,Richard H.; Et Al
    参考文献:Phytochemistry (Elsevier) 日期:2016 卷标:122 页码:11-21]

    821-41-0 = 928-92-7
    反应条件:1.1 Reagents: (Ethenyloxy)Trimethylsilane Catalysts: Grubbs Second Generation Catalyst Solvents: Dichloromethane; 1.5 H,Reflux
    标题:Development Of Isomerization And Cycloisomerization With Use Of A Ruthenium Hydride With N-Heterocyclic Carbene And Its Application To The Synthesis Of Heterocycles
    作者:Arisawa,Mitsuhiro; Terada,Yukiyoshi; Takahashi,Kazuyuki; Nakagawa,Masako; Nishida,Atsushi
    参考文献:Journal Of Organic Chemistry 日期:2006 卷标:71(11) 页码:4255-4261]

    31535-05-4 = 928-92-7
    反应条件:1.1 Reagents: Sodium Solvents: Diethyl Ether,P-Xylene
    标题:Synthesis Of (+/-)-Brevioxime And (+/-)-Puraquinonic Acid And Studies On Peptide Ligation And Acyl Transfer
    作者:Hisaindee,Soleiman
    参考文献:2003 卷标:64(7)]

    53107-05-4 = 928-92-7
    反应条件:1.1 Reagents: Magnesium Solvents: Diethyl Ether
    标题:Magnesium Ring Scission Reaction Of 2-Alkyl-3-Chlorotetrahydropyran
    作者:Ding,Xinteng; Ge,Yu; Teng,Zhu; Fan,Junyao
    参考文献:Huaxue Xuebao 日期:1987 卷标:45(11) 页码:1138-9]

    34495-74-4 = 928-92-7
    反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Tetrahydrofuran
    标题:Iron-Catalyzed Intramolecular Allylic C-H Amination
    作者:Paradine,Shauna M.; White,M. Christina
    参考文献:Journal Of The American Chemical Society 日期:2012 卷标:134(4) 页码:2036-2039]

    34495-74-4 = 928-92-7
    反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether
    标题:Catalytic Epoxidation Of Alkenes With Oxone
    作者:Denmark,Scott E.; Forbes,David C.; Hays,David S.; Depue,Jeffrey S.; Wilde,Richard G.
    参考文献:Journal Of Organic Chemistry 日期:1995 卷标:60(5) 页码:1391-407]

    110-87-2 = 928-92-7
    反应条件:1.1 Reagents: Sodium,Chlorine Solvents: Diethyl Ether
    标题:(E)-4-Hexen-1-Ol
    作者:Paul,Raymond; Riobe,Olivier; Maumy,Michel
    参考文献:Organic Syntheses 日期:1976 卷标:55 页码:62-7]

    34495-74-4 = 928-92-7
    反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Tert-Butyl Methyl Ether; Overnight,Rt1.2 Reagents: Sulfuric Acid Solvents: Water
    标题:Iodide-Catalyzed Cyclization Of Unsaturated N-Chloroamines: A New Way To Synthesize 3-Chloropiperidines
    作者:Noack,Michael; Gottlich,Richard
    参考文献:European Journal Of Organic Chemistry 日期:2002 卷标:(18) 页码:3171-3178]

    156051-16-0 = 928-92-7
    反应条件:1.1 Reagents: Sodium Solvents: Diisopropyl Ether
    标题:The Synthesis Of Some 4-Alken-1-Ols
    作者:Brandon,Richard C.; Derfer,John M.; Boord,Cecil E.
    参考文献:Journal Of The American Chemical Society 日期:1950 卷标:72 页码:2120-2]

    34495-74-4 = 928-92-7
    反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Tetrahydrofuran; 30 Min,0 °C; 0 °C -> Rt; 5 Min,Rt1.2 Reagents: Sodium Sulfate Solvents: Water; 0 °C
    标题:Total Synthesis And Biological Evaluation Of Siladenoserinol A And Its Analogues
    作者:Yoshida,Masahito; Saito,Koya; Kato,Hikaru; Tsukamoto,Sachiko; Doi,Takayuki
    参考文献:Angewandte Chemie 日期:2018 卷标:57(18) 页码:5147-5150]

    5371-52-8 + 4736-60-1 = 928-92-7
    反应条件:1.1 Reagents: Potassium Tert-Butoxide Solvents: Tetrahydrofuran; -78 °C
    标题:Highly Functionalized And Potent Antiviral Cyclopentane Derivatives Formed By A Tandem Process Consisting Of Organometallic,Transition-Metal-Catalyzed,And Radical Reaction Steps
    作者:Jagtap,Pratap R.; Ford,Leigh; Deister,Elmar; Pohl,Radek; Cisarova,Ivana; Et Al
    参考文献:Chemistry - A European Journal 日期:2014 卷标:20(33) 页码:10298-10304]

    917-54-4 + 110-87-2 = 928-92-7 [标题:Reaction Conditions
    标题:Preparation And Application Of Thermo-Color Materials Based On Heat Sensitive Dyestuffs
    作者:Guo,Jiazhen; Cheng,Qichao; Liu,Zhengtang
    参考文献:Huagong Jinzhan 日期:1997 卷标:(6) 页码:57-59]

    25166-87-4 = 928-92-7
    反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Diethyl Ether
    标题:Intramolecular N-Alkenylnitrone Additions. Regio- And Stereochemistry
    作者:Oppolzer,W.; Siles,S.; Snowden,R. L.; Bakker,B. H.; Petrzilka,M.
    参考文献:Tetrahedron 日期:1985 卷标:41(17) 页码:3497-509
📜5-己烯-1-醇置于c24H42N2Pru(1+)*f6P(1-)体系中,用 氘代丙酮 作为反应溶剂,化学反应 0.25H,以96%的收率获得产物4-己烯-1-醇
参考文献:在形式上16电子的cp *孺咪唑基取代的动态π键(K 2-P,ñ)+催化剂允许惊人的速度增加(ë)-选择性monoisomerization烯烃的
标题:在形式上16电子的cp *孺咪唑基取代的动态π键(K 2-P,ñ)+催化剂允许惊人的速度增加(ë)-选择性monoisomerization烯烃的
摘要:烯烃异构化可以是一种原子经济的方法,可用于反应生成范围广泛的用于合成的烯烃中间体,但是完全平衡的二取代内部烯烃的混合物通常包含大量的位置异构体和几何异构体(e和z).用于烯烃异构化的大多数经典催化剂体系都难以动力学控制位置异构或e / Z异构.我们报告了配位不饱和,形式为16电子的cp * Ru催化剂5,它可促进线性1-烯烃同时向其内部类似物进行区域和立体选择性异构化,从而提供(e)-2-烯烃大于95%.由于无腈催化剂5比以前发表的含腈类似物2 + 2A快400倍以上,因此在15分钟至4小时内完成5个完全环境温度反应的0.1-0.5摩尔%非常合理的负载量.的uv-Vis,NMR,和计算研究描绘K上膦作为hemilabile,四-电子给体的咪唑基片段2-P,ñ协调.对于第一次,我们显示直接的实验证据表明,Pn配体已经通过表征中间的cp *茹[η接受从基板的质子3-烯丙基] [K 1-P)pn+
DOI:10.1021/acscatal.8B04345

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