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Merck
모든 사진(3)

주요 문서

366315

Sigma-Aldrich

Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct

동의어(들):

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 코드:
12161600
PubChem Substance ID:
NACRES:
NA.22

양식

solid

반응 적합성

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

일반 설명

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

애플리케이션

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.

픽토그램

Health hazardExclamation mark

신호어

Warning

유해 및 위험 성명서

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

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

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)

문서

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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