CAS: 42196-31-6; Palladium(Ii) 2,2,2-Trifluoroacetate

该化合物是与配方Pd(CFCOO)的协调化合物,该配方是+2氧化状态中的,该配方一般是白到光黄色固态,以其在各种有机反应中作为催化剂的作用而著称,特别是在诸如铃木和Heck反应等交叉反应中.三氟丙烷酸是强大的电子带色组,它们增强了中心的再活性.三氟乙酸铵(II)是有机溶剂中的溶解物,适合有机合成使用.重要的是要谨慎地处理这一化合物,因为化合物可能有毒,并可能对环境造成危害.此外,它对于湿气很敏感,应储存在干燥环境中以保持其稳定性.

结构式图片

欧盟法规

C&L通报

合成工艺路线路线简述

    醋酸钯,三氟乙酸置于三氟乙酸,三氟乙酸钯体系中,用to Afford 1.3 G Of Brown Product,I.E. Palladium (II) Trifluoroacetate,Mp 210oc. (Dec)的收率获得产物三氟乙酸钯
    参考文献:Intermediate Phenolic Compounds For The Catalytic Synthesis Of Chromans
    标题:Intermediate Phenolic Compounds For The Catalytic Synthesis Of Chromans
    摘要:一种催化合成光学活性或外消旋的香豆素,包括其中间体;该合成采用不对称钯(II)催化的氧化环化反应,反应物为2-同烯基苯酚,提供了制备香豆素的有用中间体,特别是制备光学活性或外消旋的维生素e.

    海关参考信息

    专利信息


    专利号:US-4598160-A
    优先权日:1983-07-15
    标题 :Intermediate phenolic compounds for the catalytic synthesis of chromans
    发明人:TRUESDALE LARRY K
    权利人:HOFFMANN LA ROCHE
    摘要:A catalytic synthesis of chromans in racemic or optically active forms, including intermediates thereto; the synthesis employs an asymmetric palladium (II) catalyzed oxidative cyclization of a 2-homoallylphenol and provides intermediates useful in making chromans, especially vitamin E in racemic or optically active forms.

    专利号:US-12221452-B2
    优先权日:2017-10-04
    标题:Synthesis of cantharidin
    发明人:DAVIDSON MATTHEW GENE; EKLOV BRIAN MATTHEW; WUTS PETER; LOERTSCHER BRAD MELVIN; SCHOW STEVEN R
    权利人:VERRICA PHARMACEUTICALS INC
    摘要:The invention provides synthetic methods for the preparation of cantharidin and analogs thereof. In one aspect, the invention provides an improved Diels-Alder cycloaddition to generate a key intermediate en route to cantharidin and analogs thereof. In certain embodiments, the new Diels-Alder reaction involves reacting Compound (2) in the presence of furan, and in the absence of acid or increased pressure, in an aprotic polar solvent with slight warming, to yield Compound (1) in favorable yield and exo-endo ratio. In another aspect, the invention also provides a new Diels-Alder reaction between compounds of Formula (III) and furan to yield compounds of Formula (IV), which can then be transformed into cantharidin or analogs thereof. In yet another aspect, the invention describes a new palladium-mediated carbonylation providing another key intermediate en route to cantharidin and analogs thereof. In addition to synthetic methods, present invention also provides compounds (i.e., intermediates) useful in the synthesis of cantharidin and analogs thereof. Compounds provided herein may have biological activity, and therefore may be used in the treatment of diseases or conditions (e.g., infectious diseases and skin conditions).

    专利号:US-8283476-B2
    优先权日:2007-06-26
    标 题:Transition metal catalyzed synthesis of 2H-indazoles
    发明人:HALLAND NIS; NAZARE MARC; LINDENSCHMIDT ANDREAS; ALONSO JORGE; RKYEK OMAR; URMANN MATTHIAS
    权利人:HALLAND NIS; NAZARE MARC; LINDENSCHMIDT ANDREAS; ALONSO JORGE; RKYEK OMAR; URMANN MATTHIAS; SANOFI SA
    摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, n nwherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct transition metal catalyzed process to a wide variety of multifunctional 2H-indazoles or 2H-azaindazoles of the formula (I) from 2-halo-phenylacetylenes or (2-sulfonato)phenylacetylenes and monosubstituted hydrazines.

    专利号:US-8026375-B2
    优先权日:2007-04-13
    标题:Transition metal catalyzed synthesis of N-aminoindoles
    发明人:HALLAND NIS; NAZARE MARC; LINDENSCHMIDT ANDREAS; RKYEK OMAR; URMANN MATTHIAS; ALONSO JORGE
    权利人:SANOFI AVENTIS
    摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, n nwherein R0; R1; R2; R3; R4; R5; R6; A1; A2; A3; A4, Q, T and J have the meanings indicated in the claims. The present invention provides a direct transition metal catalyzed process to a wide variety of multifunctional N-aminoindole or N-amino-azaindoles of the formula I from 2-halo-phenylacetylenes or (2-sulfonato)phenyl-acetylenes and N,N-disubstituted hydrazines, useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides.

    专利号:US-2023174477-A1
    优先权日:2021-12-03
    标题:Methods for synthesis of the tricyclic prostaglandin d2 metabolite methyl ester
    发明人:DAI MINGJI; SIMS HUNTER
    权利人:PURDUE RESEARCH FOUNDATION
    摘要:Methods for the synthesis of a tricyclic-prostaglandin D 2 metabolite methyl ester or a pharmaceutically acceptable salt thereof.

    专利号:US-8188282-B2
    优先权日:2006-07-15
    标 题:Regioselective palladium catalyzed synthesis of benzimidazoles and azabenzimidazoles
    发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARE MARC; HALLAND NIS; RKYEK OMAR; URMANN MATTHIAS
    权利人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARE MARC; HALLAND NIS; RKYEK OMAR; URMANN MATTHIAS; SANOFI AVENTIS
    摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, n nwherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct palladium catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides.
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