CAS: 768-70-7; 3-Ethynylanisole

该化合物是一种有机化合物,其特征是苯乙炔结构,在苯环的元位置上以甲氧基组替代,该化合物在苯环的元位置上一般是一种无色的黄色液体,以其芳香特性而著称.该化合物的分子式为C10H10O,表明存在一种可提高其有机溶剂溶解度的甲氧基组(-OCH3),该化合物显示出乙炔细胞碳原子之间的三重结合,有助于其在各种化学反应中的再活性,例如混合反应和核生殖添加.3-甲基苯乙烯用于有机合成和材料科学,特别是在开发功能化聚合物和作为更复杂的有机分子的构件.该化合物的特性,包括沸点和密度,可因纯度和环境条件而变化.许多有机化合物,适当的处理和安全防范措施对于潜在的毒性和易燃性至关重要.

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上下游产品

3-(3-甲氧基苯基)-2-丙炔-1-醇 3-(3-Methoxyphenyl)Prop-2-Yn-1-Ol 27913-19-5
(3-甲氧基苯基乙炔)三甲基硅烷 3-(Trimethylsilylethynyl)Anisole 40230-92-0
3-(3-Methoxyphenyl)Propiolic Acid 7621-89-8
3-甲氧基苯甲醛 3-Methoxy-Benzaldehyde 591-31-1

合成工艺路线路线简述

    📜间溴苯甲醚置于bis-Triphenylphosphine-Palladium(II) Chloride,Copper(L) Iodide,Potassium Carbonate,三乙胺体系中,用 四氢呋喃,甲醇 作为反应溶剂,化学反应 34.0H,反应生成 3-乙炔基苯甲醚
    参考文献:高选择性且无添加剂的 Pd(Oac)2/cpp 催化炔烃的氢氨基羰基化
    标题:高选择性且无添加剂的 Pd(Oac)2/cpp 催化炔烃的氢氨基羰基化
    摘要:在此,报道了使用 Pd 通过炔烃与各种胺底物(如芳香胺,脂肪胺,固体胺源如 Nh 4 Hco 3,甚至强碱性哌啶)的氢氨基羰基化反应合成支链 α,β-不饱和酰胺. (Oac) 2 /混合n-杂环卡宾-膦-膦(Cpp)催化体系.该反应具有无添加剂,底物范围广,选择性高(b/l > 99 : 1)和优异的产率的特点.机理研究表明该反应通过氢化钯途径发生的. Cpp采用卡宾-膦配位模式的杂化二齿配体构象,其中一个磷原子保持外部可接近,可能在催化循环过程中充当稳定辅助剂.
    DOI:10.1039/d4Ob00644E

    海关参考信息

    专利信息


    专利号:US-10829792-B2
    优先权日:2017-03-21
    标 题 :Biocatalytic synthesis of strained carbocycles
    发明人:CHEN KAI; HUANG XIONGYI; KAN S B JENNIFER
    权利人:CALIFORNIA INST OF TECHN
    摘要:Provided herein are methods for producing products containing strained carbocycles, such as cyclopropene moieties and/or bicyclobutane moieties. The methods include combining an alkyne and a carbene precursor in the presence of a heme protein, e.g., a cytochrome P450, under conditions sufficient to form the strained carbocycle. Reaction mixtures for producing strained carbocycles are also described, as well as whole-cell catalysts comprising heme proteins and variants thereof for forming cyclopropenes, bicyclobutanes, and related products.

    专利号:US-8835658-B2
    优先权日:2012-12-28
    标 题:Asymmetric synthesis of norcantharidin analougus by alkynylation of oxabenzonorbornadienes and their anticancer activities
    发明人:CHAN ALBERT SUN-CHI; FAN BAOMIN; WANG JUN; LIN CHENGYUAN; HUANG CHAO; YANG QINGJING; XU JIANBIN; BIAN ZHAOXIANG; LU AIPING; HU JUN
    权利人:UNIV HONG KONG BAPTIST; UNIV YUNNAN NATIONALITIES
    摘要:The present invention relates to a type of norcantharidin analogues and a method to synthesis such norcantharidin analogues by transition metal-catalyzed alkynylation of 7-oxabenzonorbornadienes. The present invention also relates to the use of such norcantharidin analogues in manufacture of a medicament for the treatment of cancer tumors.

    专利号:US-7402703-B2
    优先权日:2005-06-08
    标 题:Stereoselective synthesis of (E)-vinylboronic esters via a Zr mediated hydroboration of alkynes
    发明人:WANG YANONG DANIEL
    权利人:WYETH CORP
    摘要:There is herein provided a process for Zr-mediated hydroboration of alkynes which offers (E)-vinylboronic esters in high yield with stereoselectivity and regioselectivity.

    专利号:US-2006281943-A1
    优先权日:2005-06-08
    标题 :Stereoselective synthesis of (E)-vinylboronic esters via a Zr mediated hydroboration of alkynes

    专利号:WO-2006132896-A2
    优先权日:2005-06-08
    标题:Stereoselective synthesis of (e)-vinylboronic esters via a zr mediated hydroboration of alkynes

    专利号:US-2014187801-A1
    优先权日:2012-12-28
    标题:Asymetric synthesis of norcantharidin analougus by alkynylation of oxabenzonorbornadienes and their anticancer activities

    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

    合成参考文献


    摘要:Merino, P., Science of Synthesis, (2010) 45, 302.
    摘要:Masuda, T.; Shiotsuki, M.; Sanda, F., Science of Synthesis, (2010) 45, 1423.
    摘要:Clark, R. W.; Wiskur, S. L., Science of Synthesis Knowledge Updates, (2015) 1, 16.
    摘要:Celik, I.; Hummel, S.; Kirsch, S. F., Science of Synthesis Knowledge Updates, (2019) 1, 15.
    摘要:Tymoshenko, D. O., Science of Synthesis Knowledge Updates, (2012) 3, 406.
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