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Merck
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697230

Sigma-Aldrich

[1,1′-双(二苯基膦)二茂铁]二氯化钯(II)

同義詞:

Pd(dppf)Cl2

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About This Item

線性公式:
(C17H14P)2Fe · PdCl2
CAS號碼:
分子量::
731.70
EC號碼:
MDL號碼:
分類程式碼代碼:
12161600
PubChem物質ID:
NACRES:
NA.22

形狀

powder

品質等級

反應適用性

core: palladium
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
reaction type: Buchwald-Hartwig Cross Coupling Reaction

mp

266-283 °C (lit.)

SMILES 字串

[Fe].Cl[Pd]Cl.[CH]1[CH][CH][C]([CH]1)P(c2ccccc2)c3ccccc3.[CH]4[CH][CH][C]([CH]4)P(c5ccccc5)c6ccccc6

InChI

1S/2C17H14P.2ClH.Fe.Pd/c2*1-3-9-15(10-4-1)18(17-13-7-8-14-17)16-11-5-2-6-12-16;;;;/h2*1-14H;2*1H;;/q;;;;;+2/p-2

InChI 密鑰

JCWIWBWXCVGEAN-UHFFFAOYSA-L

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應用

Pd(dppf)Cl2可作为有效的钯催化剂用于以下反应:
  • 仲烷基和正烷基格氏试剂的交叉偶联,产率和选择性高。
  • 芳基硼酸酯与[11C]甲基碘进行Suzuki偶联反应,形成官能化[11C]甲苯衍生物。
  • 1,3,5-三溴苯与格氏试剂进行Kumada交叉偶联反应,形成星形低聚噻吩。
对于小规模和高通量应用,可选用ChemBeads形式(919780)
用于C-C和C-N偶联反应的催化剂。

相關產品

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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Electrophilic activation of benzaldehydes through ortho palladation: one-pot synthesis of 3-methylene-indan-1-ols through a domino allylstannylation/Heck reaction under neutral conditions.
Ján Cvengros et al.
Angewandte Chemie (International ed. in English), 48(33), 6148-6151 (2009-07-11)
Star?Shaped Oligothiophenes for Solution?Processible Organic Field?Effect Transistors.
Ponomarenko S
Advances in Functional Materials, 13(8), 591-596 (2003)
Dichloro [1,1?-bis (diphenylphosphino) ferrocene] palladium (II): an effective catalyst for cross-coupling reaction of a secondary alkyl grignard reagent with organic halides.
Hayashi T
Tetrahedron Letters, 20(21), 1871-1874 (1979)
Shirbin, S. J. et al.
Tetrahedron Letters, 51, 2971-2971 (2010)
Julien Monot et al.
Organic letters, 11(21), 4914-4917 (2009-10-06)
Complexes of triaryl- and trialkylboranes with N-heterocyclic carbenes (NHCs) participate in Suzuki-Miyaura cross-coupling reactions and provide coupled products in good yields under base-free conditions. The reaction can be applied to Csp(2)-Csp(2) and Csp(2)-Csp(3) carbon-carbon bond formation with triflates, iodides, bromides

文章

Tandem hydroboration Suzuki Coupling both intermolecular and intramolecular gave diverse alkyl substituted products dppf

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