CAS: 958449-00-8; Potassium (Butan-2-yl)Trifluoroboranuide

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88496-88-2 897067-94-6 1138434-30-6

合成工艺路线路线简述

    📜二氟化氢钾,2-丁基硼酸频呢醇酯 以 甲醇,水 作为反应溶剂,化学反应 12.0H,反应生成 Sec-丁基三氟硼酸钾
    参考文献:锰 (Iii) 促进苯胺双羰基化合成 α-酮酰胺
    标题:锰 (Iii) 促进苯胺双羰基化合成 α-酮酰胺
    摘要:在双羰基化中使用苯胺作为亲核试剂是一个长期的挑战.在本次交流中,已经开发了一种 Mn(Iii) 促进的烷基硼酸盐或 Hantzsch 酯与苯胺的双羰基化,用于合成 α-酮酰胺.通过使用容易获得的烷基三氟硼酸钾或 Hantzsch 酯作为起始材料,并以廉价且无毒的 Mn(Oac) 3 . 2H2O 作为促进剂,以中等至非常好的收率合成了范围广泛的烷基α-酮酰胺衍生物.非常好的选择性.
    DOI:10.1002/adsc.202101233

    海关参考信息

    专利信息


    专利号:US-8513465-B2
    优先权日:2008-02-04
    标题:Potassium organotrifluoroborate derivative and a production method therefor
    发明人:KANG HEONJOONG; HAM JUNGYEOB; AHN HONG RYUL; PARK YOUNG HEE
    权利人:KANG HEONJOONG; HAM JUNGYEOB; AHN HONG RYUL; PARK YOUNG HEE; SNU R&DB FOUNDATION
    摘要:Provided are a production method for a potassium organotrifluoroborate compound having a hydroxyl group, and a novel potassium organotrifluoroborate compound having a hydroxyl group. The production method is advantageous in that a potassium organotrifluoroborate compound can be produced in a single reaction without recourse to a process of isolating and purifying an intermediate. The novel potassium organotrifluoroborate compound having a hydroxyl group is useful as a reactant which is widely used in the total synthesis of physiologically active natural products and diverse organic synthesis reactions including halogen substitution reactions, 1,2- and 1,4-addition reactions using a rhodium (Rh) catalyst, and Suzuki coupling reactions using a palladium (Pd) catalyst.

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    📌 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:Synergistic Visible-Light Photoredox/nickel-Catalyzed Synthesis Of Aliphatic Ketones Via N-C Cleavage Of Imides
    作者:Javad Amani,Rauful Alam,Shorouk Badir,Gary A. Molander |发布日期:2017.5.5
    摘要:An Electrophilic, Imide-Based, Visible-Light-Promoted Photoredox/ni-Catalyzed Cross-Coupling Reaction For The Synthesis Of Aliphatic Ketones Has Been Developed. This Protocol Proceeds Through N-C(O) Bond Activation, Made Possible Through The Lower Activation Energy For Metal Insertion Into This Bond Due To Delocalization Of The Lone Pair Of Electrons On The Nitrogen By Electron-Withdrawing Groups.

    合成参考文献


    摘要:Primer, D. N.; Molander, G. A., Science of Synthesis, (2019) , 284.
    摘要:André-Joyaux, E.; Gnägi, L.; Meléndez, C.; Soulard, V.; Renaud, P., Science of Synthesis, (2021) , 483.
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