CAS: 17216-08-9; 2-Acetyl-3,4-Dihydronaphthalen-1(2H)-One

该化合物是属于氯酮类的有机化合物,其特点是四龙结构,由含有六人芳香环和五人含碳基环的双环系统组成,其特点是四龙结构,其特点是四龙结构在四龙框架的2位置上存在乙基组,其特点是四龙框架的2位置存在一种乙基,它一般是黄到褐色液体或固体,视其纯度和形态而定. 2-乙基-1-乙酮因其在有机合成中的潜在应用以及作为各种药品和农用化学制剂的制备中的一个构件而闻名.其再活动受到碳基组的影响,使其易受到核循环伤害袭击,并可以参与各种化学反应,包括凝固和氧化.此外,它可能展示出有趣的生物活动,但对其药理特性的具体研究可能有限.

结构式图片

上下游产品

acetic anhydride 3,4-dihydronaphthalene-1(2H)-one ethyl acetate acetyl chloride 1-Phenyl-3-(1,2,3,4-tetrahydro-1-oxo-2-naphthalenyl)-1,3-propanedione 1-(4-Chlorophenyl)-3-(1,2,3,4-tetrahydro-1-oxo-2-naphthalenyl)-1,3-propanedione 1-(2,5-Dichlorophenyl)-3-(1,2,3,4-tetrahydro-1-oxo-2-naphthalenyl)-1,3-propanedione 1-(5-Chloro-2-propoxyphenyl)-3-(1,2,3,4-tetrahydro-1-oxo-2-naphthalenyl)-1,3-propanedione

合成工艺路线路线简述

    📜4-苯基丁酰氯置于硝基甲烷,Silver Perchlorate体系中,化学反应生成2-乙酰-1-四酮
    参考文献:326.强酸催化的酰化作用和相关反应.第十六部分.某些ω-苯基链烷酰基高氯酸盐的反应
    标题:326.强酸催化的酰化作用和相关反应.第十六部分.某些ω-苯基链烷酰基高氯酸盐的反应
    摘要:
    Doi:10.1039/jr9570001718

    海关参考信息

    专利信息


    专利号:US-5567830-A
    优先权日:1994-02-14
    标题 :Process for synthesis of acetylenic carbinols
    发明人:UPASANI RAVINDRA B
    权利人:COCENSYS INC
    摘要:A method for the preparation of an acetylenic alcohol by reaction of 1,2-dibromoethylene with an alkyl, aryl an heteroaryl lithium in an inert solvent, followed by reaction with a carbonyl-containing compound to give an acetylenic alcohol is disclosed.

    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:Pd-Catalyzed Alkene Difunctionalization Reactions Of Enolates For The Synthesis Of Substituted Bicyclic Cyclopentanes
    作者:Evan C. Bornowski,Elsa M. Hinds,Derick R. White,Yusuke Nakamura,John P. Wolfe |发布日期:2019.8.16
    摘要:Palladium-Catalyzed Alkene Difunctionalization Reactions Between Alkenes Bearing Tethered Aryl Or Alkenyl Triflates And Enolate Nucleophiles Are Described. The Transformations Form Two C-C Bonds, A Ring, And Up To Two Stereocenters While Producing Substituted Cyclopentane Derivatives That Contain Appended Carbonyl Functionality. Products Are Formed With Up To >20:1 Diastereoselectivity, And The Formation

    合成参考文献


    摘要:Liu, G.; Chen, P., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 2, 3.
    摘要:Uyanik, M.; Ishihara, K., Science of Synthesis: Catalytic Oxidation in Organic Synthesis, (2017) 1, 635.
    摘要:Wang, P.-S.; Sayed, M.; Gong, L.-Z., Science of Synthesis: Knowledge Updates, (2023) 1, 189.
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