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Sigma-Aldrich

Dichlorobis(tri-o-tolylphosphine)palladium(II)

97%

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Synonym(s):
PdCl2[P(o-Tol)3]2
Linear Formula:
[(CH3C6H4)3P]2PdCl2
CAS Number:
40691-33-6
Molecular Weight:
786.06
MDL number:
MFCD00274659
UNSPSC Code:
12161600
PubChem Substance ID:
24868751
NACRES:
NA.22

Quality Level

200

Assay

97%

form

solid

reaction suitability

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

mp

280 °C (dec.) (lit.)

SMILES string

Cl[Pd]Cl.Cc1ccccc1P(c2ccccc2C)c3ccccc3C.Cc4ccccc4P(c5ccccc5C)c6ccccc6C

InChI

1S/2C21H21P.2ClH.Pd/c2*1-16-10-4-7-13-19(16)22(20-14-8-5-11-17(20)2)21-15-9-6-12-18(21)3;;;/h2*4-15H,1-3H3;2*1H;/q;;;;+2/p-2

InChI key

OTYPIDNRISCWQY-UHFFFAOYSA-L

Related Categories

General description

Dichlorobis(tri-o-tolylphosphine)palladium(II) is a useful catalyst for C-C and C-N coupling reactions.

Application

Application Guide for Palladium Catalyzed Cross-Coupling Reactions

Catalyst for C-C and C-N coupling reaction.
Dichlorobis(tri-o-tolylphosphine)palladium(II) has been employed as catalyst for the following studies:
  • Reaction of tributyltin enolates, prepared in situ from tributyltin methoxide and enol acetates, with aryl bromides.
  • Coupling reaction of aryl bromides with vinylic acetates.
  • Negishi-Reformatsky coupling reaction of aryl bromides with ethyl 2-(tributylstannyl)acetates.
  • Synthesis of (E)-methyl 3-(7-indolyl)-2-methacrylate, via Heck reaction.
  • Synthesis of imidazopyrimidine derivatives.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Guram, A. S.; Buchwald, S. L
Angewandte Chemie (International Edition in English), 34, 1348-1348 (1995)
Stereoselective total synthesis of (+)-licochalcone E.
Liu Z, et al.
Archives of Pharmacal Research, 34(8), 1269-1276 (2011)
Toward the enantioselective total synthesis of lyngbyatoxin A: on the stereocontrolled introduction of the quaternary stereogenic centre.
T?nder JE and Tanner D.
Tetrahedron, 59(35), 6937-6945 (2003)
Guo-Hua Chu et al.
The open medicinal chemistry journal, 3, 8-13 (2009-12-08)
A series of imidazopyrimidine derivatives with the general formula I was synthesized and identified as potent inhibitors of iNOS dimer formation, a prerequisite for proper functioning of the enzyme. Stille and Negishi coupling reactions were used as key steps to
Guram, A. S.; Buchwald, S. L.
Journal of the American Chemical Society, 116, 7901-7901 (1994)
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