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重要文件

205869

Sigma-Aldrich

乙酸钯(II)

reagent grade, 98%

同義詞:

Pd(OAc)2

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About This Item

線性公式:
Pd(OCOCH3)2
CAS號碼:
分子量::
224.51
Beilstein:
6086766
EC號碼:
MDL號碼:
分類程式碼代碼:
12352300
PubChem物質ID:
NACRES:
NA.22

等級

reagent grade

品質等級

化驗

98%

形狀

powder

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

mp

216.3-223.7 °C (dec.)

SMILES 字串

CC(O[Pd]OC(C)=O)=O

InChI

1S/2C2H4O2.Pd/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2

InChI 密鑰

YJVFFLUZDVXJQI-UHFFFAOYSA-L

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一般說明

[Pd(OAc)2]3 是一种钯配位络合物,也是一种多相金属催化剂,它被广泛用于有机合成中,比如转移金属化、插入反应、氧化加成反应、芳基卤化物的直接均偶联、 形成C-N的Buchwald-Hartwig 反应、炔烃的还原和还原消除反应。它还可用作合成其他 Pd(II)化合物的起始材料,以及制备用于Suzuki-Miyaura交叉偶联和C-H官能化反应的活性钯催化剂。

應用

[Pd(OAc)2]3 可被用作:
  • 催化剂,用于末端和内部炔烃的区域选择性抗氢氯化反应。
  • 前体,用于制备Heck偶联反应和Sonogashira交叉偶联反应用的非均相钯络合物催化剂。

相關產品

產品號碼
描述
訂價

訊號詞

Danger

危險聲明

危險分類

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Sens. 1A

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

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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分析證明 (COA)

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存取文件庫

Mark McLaughlin et al.
Organic letters, 8(15), 3311-3314 (2006-07-14)
[Structure: see text] An efficient regioselective method for the preparation of structurally diverse imidazopyridinones and benzoimidazolones starting from readily available and economical starting materials is described. High-yielding reductive alkylation of electron-deficient o-haloarylamines followed by treatment with inexpensive N-chlorosulfonyl isocyanate afforded
Wolfe, J. P.; Buchwald, S. L.
The Journal of Organic Chemistry, 62, 1264-1264 (1997)
Mark S Chen et al.
Journal of the American Chemical Society, 126(5), 1346-1347 (2004-02-05)
Sulfoxide ligation to Pd(II) salts is shown to selectively promote C-H oxidation versus Wacker oxidation chemistry and to control the regioselectivity in the C-H oxidation products. A catalytic method for the direct C-H oxidation of monosubstituted olefins to linear (E)-allylic
Ikuyo Kamiya et al.
The Journal of organic chemistry, 70(2), 696-698 (2005-01-18)
A highly regioselective hydroselenation of terminal alkynes with benzeneselenol can be achieved by the combination of palladium acetate and pyridine, providing the corresponding terminal alkenes, (i.e., 2-phenylseleno-1-alkenes) as a sole product. In this hydroselenation, pyridine may act as a suitable
Brunner, M.; Alper, H
The Journal of Organic Chemistry, 62, 7565-7565 (1997)

文章

A variety of transition-metal catalysts for the Suzuki coupling reaction are now available in our catalog. The majority of these catalysts are palladium- and nickelbased, typically utilizing phosphine-derived ligands.

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