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Merck
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文件

708739

Sigma-Aldrich

tBuXPhos Pd G1

别名:

t-BuXPhos palladium(II) phenethylamine chloride, tBuXPhos-Pd-G1, [2-(二叔丁基膦)-2′,4′,6′-三异丙基-1,1′-联苯基][2-(2-氨基乙基)苯基)]氯化钯(II), t-BuXPhos预催化剂, 氯[2-(二叔丁基膦)-2′,4′,6′-三异丙基-1,1′-联苯基][2-(2-氨基乙基)苯基)]钯(II), 氯[2-(二叔丁基膦基)-2',4',6'-三异丙基-1,1'-联苯基][2-(2-氨基乙基)苯基)]钯(II)

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About This Item

经验公式（希尔记法）:
C37H55ClNPPd
CAS号:
1142811-12-8
分子量:
686.69
MDL號碼:
MFCD12911909
分類程式碼代碼:
12161600
PubChem物質ID:
329762821
NACRES:
NA.22

形狀

solid

特點

generation 1

反應適用性

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

150-159 °C

官能基

phosphine

SMILES 字串

NCCc1ccccc1[Pd]Cl.CC(C)c2cc(C(C)C)c(c(c2)C(C)C)-c3ccccc3P(C(C)(C)C)C(C)(C)C

InChI

1S/C29H45P.C8H10N.ClH.Pd/c1-19(2)22-17-24(20(3)4)27(25(18-22)21(5)6)23-15-13-14-16-26(23)30(28(7,8)9)29(10,11)12;9-7-6-8-4-2-1-3-5-8;;/h13-21H,1-12H3;1-4H,6-7,9H2;1H;/q;;;+1/p-1

InChI 密鑰

LQRWNWRVOIDQOD-UHFFFAOYSA-M

相关类别

應用

钯催化交叉偶联反应应用指南
C-C键和C-N键形成的催化剂。

法律資訊

用法以美国专利 6307087 和 6395916 为准。

象形圖

Health hazardExclamation mark
GHS08,GHS07

訊號詞

Warning

危險分類

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

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

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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Brian K Lee et al.
Tetrahedron letters, 50(26), 3672-3674 (2009-07-01)
Simple and efficient procedures for the Pd-catalyzed cross-coupling reaction of aryl chlorides and dimethylamine are described. At room temperature with a strong base, t-BuXPhos is employed as the supporting ligand; at 110 °C with a weak base, XPhos is employed
Mark R Biscoe et al.
Organic letters, 11(8), 1773-1775 (2009-03-20)
Simple, efficient procedures for the monoarylation of acetate esters and aryl methyl ketones using aryl chlorides are presented. Previously, no general method was available to ensure the highly selective monoarylation of these classes of substrates using aryl chlorides. Using palladium
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
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
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

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