CAS: 59820-90-5; 1-(7-Bromo-2,3-Dihydrobenzo[b][1,4]Dioxin-6-yl)Ethanone

该化合物是一个化学化合物,其独特结构包括一种苯二恶英和一个可功能组;该化合物具有溴原子特征,有助于其再活性和在有机合成中的潜在应用;该二恶英结构的存在表明,它可能展示出有趣的生物活动,因为含有这一框架的许多化合物因其药理特性而闻名.埃太酮组表示,它是一种可参与各种化学反应的氯酮,例如核肺病添加物.此外,该化合物的分子结构可能会影响其溶性,稳定性和与其他化学物种的相互作用.

结构式图片

上下游产品

benzo-1,4-dioxane 6,7-dibromo-2,3-dihydrobenzo[b][1,4]dioxine acetyl chloride 6-bromo-7-chloro-2,3-dihydro-benzo[1,4]dioxine

合成工艺路线路线简述

    📜乙酰氯,6-溴-1,4-苯并恶烷置于aluminum (Iii) Chloride体系中,用 四氯化碳 作为反应溶剂,以69%的收率获得产物1-(7-溴-2,3-二氢-1,4-苯并二氧六环-6-基)乙酮
    参考文献:O-Acylbenzonitriles: Synthesis And Heterocyclization Under Acid Hydrolysis Of The Cyano Group
    标题:O-Acylbenzonitriles: Synthesis And Heterocyclization Under Acid Hydrolysis Of The Cyano Group
    摘要:2-Cyanobenzophenones Were Synthesized By Reaction Of 2-Bromobenzophenones With Copper(I) Cyanide In Dmf,And Their Transformations Involving Acid Hydrolysis Of The Cyano Group Were Studied. Reactions Of O-Benzoylbenzonitriles With Trifluoroacetic Acid In The Presence Or In The Absence Of Sulfuric Acid Afforded 3-Hydroxyphthalimidines In High Yields. Under Analogous Conditions,Benzonitriles Having No Acyl Group In The Ortho Position Were Converted To The Corresponding Benzamides. 2-Cyanobenzophenones Reacted With Sulfuric Acid In The Absence Of Trifluoroacetic Acid To Give Only Substituted Anthraquinones.
    DOI:10.1134/s1070428018030065

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献

    参考DOI号:10.1134/S1070428018030065
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