CAS: 83237-27-8; 1-(2-Hydroxyethyl)Cyclobutan-1-Ol

该化合物是一种双功能环丁烷衍生物,主要包括一个主要氢氧基组和一个附属于环丁烷环的二级氢氧基组,这种结构具有独特的反应性,使其成为有机合成的多功能中间体,特别是用于制造环和多功能化合物.存在两个氢氧基组,可以有选择地发挥作用,使药物,农用化学品和特殊聚合物的应用成为可能.其硬性环丁烷核心助长了消毒性限制,可以利用这些限制影响目标分子的相容稳定性.该化合物的平衡的氢能性和中度极性增强了其在普通有机溶剂中的溶性,促进了其在多步骤合成途径中的使用.

结构式图片

相似化合物

933695-45-5 83237-26-7 141227-29-4

欧盟法规

C&L通报

上下游产品

methanol nonane5,7-dioxaspiro3.5nonane 1-oxa-spiro[2.3]hexane-2-carboxylic acid ethyl ester diethoxyphosphoryl-acetic acid ethyl ester 2-(1-hydroxycyclobutyl)ethyl 4-methylbenzenesulfonate 4-oxa-5-phenylspiro[3.4]°Ctane

合成工艺路线路线简述

  • 1120-56-5 = 83237-27-8
    反应条件:1.1 Reagents: Sulfuric Acid2.1 Reagents: Sulfuric Acid Catalysts: Methanol
    标题:Synthesis Of 1-Vinylcyclobutene From Methylenecyclobutane Based On The Prins Reaction
    作者:Finkel'Shtein,E. Sh.; Et Al
    参考文献:Izvestiya Akademii Nauk Sssr 日期:1982 卷标:(7) 页码:1665-6]

    73637-29-3 = 83237-27-8
    反应条件:1.1 Reagents: Sulfuric Acid Catalysts: Methanol
    标题:Synthesis Of 1-Vinylcyclobutene From Methylenecyclobutane Based On The Prins Reaction
    作者:Finkel'Shtein,E. Sh.; Et Al
    参考文献:Izvestiya Akademii Nauk Sssr 日期:1982 卷标:(7) 页码:1665-6]

    73637-29-3 = 83237-27-8 + 83237-26-7
    反应条件:1.1 Reagents: Methanol Catalysts: Sulfuric Acid Solvents: Methanol
    标题:Electrophilic Addition To Methylenecyclobutane And Bicyclobutylidene
    作者:Finkel'Shtein,E. Sh.; Et Al
    参考文献:Neftekhimiya 日期:1985 卷标:25(1) 页码:48-57]

    1120-56-5 = 83237-27-8 + 83237-26-7
    反应条件:1.1 Catalysts: Sulfuric Acid Solvents: Water2.1 Reagents: Methanol Catalysts: Sulfuric Acid Solvents: Methanol
    标题:Electrophilic Addition To Methylenecyclobutane And Bicyclobutylidene
    作者:Finkel'Shtein,E. Sh.; Et Al
    参考文献:Neftekhimiya 日期:1985 卷标:25(1) 页码:48-57
📜1-Oxaspiro<2.5>Hexan-2-Carbonsaeure-Ethylester,3,3-Trimethylen-Glycidsaeure-Ethyl-Ester置于lithium Aluminium Tetrahydride体系中,用 四氢呋喃,乙醚 作为反应溶剂,化学反应 7.0H,反应生成 1-(2-羟基乙基)环丁醇
参考文献:Ep2011788
标题:Ep2011788

海关参考信息

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:A New Approach To The Synthesis Of 1-Oxaspiro[4.N]Alkanes And Tetrahydrofurans By The 1,5-Ch Insertion Reaction Of Magnesium Carbenoids
作者:Tsuyoshi Satoh,Tsukasa Yasoshima,Hitoshi Momochi |发布日期:2012.4
摘要:In High To Quantitative Yields Via The 1,5-Ch Insertion Reaction Of Generated Magnesium Carbenoid Intermediates. When This Procedure Was Commenced With Acyclic Ketones, Multi-Substituted Tetrahydrofurans Were Obtained In Up To A 96% Yield. This Procedure Provides A New And Good Way For The Synthesis Of 1-Oxaspiro[4.N]Alkanes And Tetrahydrofurans With The Formation Of A Carbon-Carbon Bond Between A Carbenoid

合成参考文献


参考文献:10.1007/bf00954189
摘要:Finkel'shtein ES, Yatsenko MS, Vdovin VM. Preparation of 1 -vinylcyclobutene from methylenecyclobutane by the prins reaction. Russian Chemical Bulletin. 1982 Jul;31(7):1483–4. doi: 10.1007/bf00954189.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知