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366315

Sigma-Aldrich

Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct

Synonym(s):

Dipalladium-tris(dibenzylideneacetone)chloroform complex, Pd2(dba)3 · CHCl3

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About This Item

Linear Formula:
(C6H5CH=CHCOCH=CHC6H5)3Pd2 · CHCl3
CAS Number:
Molecular Weight:
1035.10
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

form

solid

reaction suitability

core: palladium
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

mp

131-135 °C (lit.)

SMILES string

[Pd].[Pd].ClC(Cl)Cl.O=C(/C=C/c1ccccc1)\C=C\c2ccccc2.O=C(/C=C/c3ccccc3)\C=C\c4ccccc4.O=C(\C=C\c5ccccc5)/C=C/c6ccccc6

InChI

1S/3C17H14O.CHCl3.2Pd/c3*18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16;2-1(3)4;;/h3*1-14H;1H;;/b3*13-11+,14-12+;;;

InChI key

LNAMMBFJMYMQTO-FNEBRGMMSA-N

General description

Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct (Pd2dba3·CHCl3) is reported to serve as effective precatalysts, or precursors to the active Pd(0) catalyst.

Application

Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct (Pd2dba3·CHCl3) was used in the following studies:
  • To compose the catalytic system for the preparation of homoallylpalladium complexes.These complexes underwent in situ Stille type cross coupling with various vinyltin reagents to afford the cyclized products bearing allyl appendages.
  • As palladium source in the asymmetric transformations of 3,4-epoxy-1-butene.
  • As catalyst for the Heck cross-coupling reaction of iodobenzene with styrene.
  • As cyclization catalyst.
  • As catalyst for [2+2+2] cycloaddtion of didehydrotriphenylenes to the corresponding extended triphenylenes.
  • As catalyst for the carbonylation of b,b-imidoyl iodides to the corresponding imidate esters used, in turn, to prepare cyclic, quaternary amino acids.

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

366315-1G:
366315-BULK:
366315-250MG:
366315-VAR:


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Palladate salts from ionic liquids as catalysts in the Heck reaction.
Gayet M,et al.
ARKIVOC (Gainesville, FL, United States), 17, 61-76 (2008)
The Journal of Organic Chemistry, 55, 3388-3388 (1990)
Tetrahedron Letters, 30, 651-651 (1989)
Palladium (II)-catalyzed tandem cyclic carbopalladation-vinylation of enyne compounds.
Yamada H, et al.
Tetrahedron Letters, 38(17), 3027-3030 (1997)
Chemistry (Weinheim An Der Bergstrasse, Germany), 12, 5657-5657 (2006)

Articles

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.

The Heck reaction is the palladium catalyzed cross-coupling reaction between alkenes and aryl or vinyl halides (or triflates) to afford substituted alkenes.

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