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Merck
CN
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文件

707589

Sigma-Aldrich

氯-（2-二环己基膦-2′,6'-双异丙氧基-1,1′-联苯） [2-（2-氨乙基）苯基] 钯 (Ⅱ)-甲基--叔 -丁醚加合物

95%

别名:

(RuPhos) 钯 (II) 氯化苯乙胺（1:1 MTBE 溶剂化物）, RuPhos Palladacycle, RuPhos 预催化剂

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About This Item

经验公式（希尔记法）:
C38H53ClNO2PPd · CH3OC4H9
CAS号:
2361069-97-6
分子量:
816.83
MDL编号:
MFCD12545955
UNSPSC代码:
12161600
PubChem化学物质编号:
329762732
NACRES:
NA.22

质量水平

100

检测方案

95%

形式

solid

特点

generation 1

反应适用性

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
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: Cross Couplings

mp

180-200 °C

官能团

phosphine

SMILES字符串

COC(C)(C)C.NCCc1ccccc1[Pd]Cl.CC(C)Oc2cccc(OC(C)C)c2-c3ccccc3P(C4CCCCC4)C5CCCCC5

InChI

1S/C30H43O2P.C8H10N.C5H12O.ClH.Pd/c1-22(2)31-27-19-13-20-28(32-23(3)4)30(27)26-18-11-12-21-29(26)33(24-14-7-5-8-15-24)25-16-9-6-10-17-25;9-7-6-8-4-2-1-3-5-8;1-5(2,3)6-4;;/h11-13,18-25H,5-10,14-17H2,1-4H3;1-4H,6-7,9H2;1-4H3;1H;/q;;;;+1/p-1

InChI key

OMMPYFRVDWZBNR-UHFFFAOYSA-M

相关类别

应用

钯催化交叉偶联反应的应用指南
用于 Buchwald-Hartwig 胺化反应的催化剂。

法律信息

用法以美国专利 6307087 和 6395916 为准。

象形图

CorrosionExclamation mark
GHS05,GHS07

警示用语：

Danger

危险声明

H314,H335

危险分类

Skin Corr. 1B - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Jaclyn L Henderson et al.
Organic letters, 12(20), 4438-4441 (2010-09-24)
Simple and efficient procedures for the Pd-catalyzed cross-coupling of primary and secondary amines with halo-7-azaindoles(pyrrolo[2,3-b]pyridine) are presented. Previously, no general method was available to ensure the highly selective reaction of the heteroaryl halide in the presence of the unprotected azaindole
Mark R Biscoe et al.
Journal of the American Chemical Society, 130(21), 6686-6687 (2008-05-02)
A new class of one-component Pd precatalysts bearing biarylphosphine ligands is described. These precatalysts are air- and thermally stable, are easily activated under normal reaction conditions at or below room temperature, and ensure the formation of the highly active monoligated
David S Surry et al.
Angewandte Chemie (International ed. in English), 47(34), 6338-6361 (2008-07-30)
Palladium-catalyzed amination reactions of aryl halides have undergone rapid development in the last 12 years, largely driven by the implementation of new classes of ligands. Biaryl phosphanes have proven to provide especially active catalysts in this context. This Review discusses
David S Surry et al.
Chemical science, 2(1), 27-50 (2011-01-01)
Dialkylbiaryl phosphines are a valuable class of ligand for Pd-catalyzed amination reactions and have been applied in a range of contexts. This review attempts to aid the reader in the selection of the best choice of reaction conditions and ligand
Ruben Martin et al.
Accounts of chemical research, 41(11), 1461-1473 (2008-07-16)
The cores of many types of polymers, ligands, natural products, and pharmaceuticals contain biaryl or substituted aromatic structures, and efficient methods of synthesizing these structures are crucial to the work of a broad spectrum of organic chemists. Recently, Pd-catalyzed carbon-carbon

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