Palladium(II) chloride

Palladium(II) chloride (PdCl2) reacts with unsubstituted or alkyl-substituted cyclic ketones in the CO atmosphere to afford acyclic diesters and acyclic chloro-substituted monoesters.[] PdCl2 reacts with N,N-dimethylallylamine in methanol to afford di-μ-chloro-bis(2-methoxy-3-N,N-dimethylaminopropyl)dipalladium(II).[] Palladium dichloride, acetate and acetylacetonate in the [bmim][BF4] or [bmim][PF6] (where[bmim]+ = 1-butyl-3-methylimidazolium cation) ionic liquids have been employed for the hydrodimerization of butadiene to form octa-2,7-dien-1-ol.[] Palladium(II) chloride is used as an oxidizing agent[] and catalyst for the Suzuki-Miyaura[] and Mizoroki-Heck reactions.[]

Application Guide for Palladium Catalyzed Cross-Coupling Reactions

Used in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar.

Application Guide for Palladium Catalyzed Cross-Coupling Reactions Used in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar. Palladium(II) chloride (PdCl2) was used in the following studies: As catalyst for the carbonylation of organic tellurides by reaction with carbon monoxide.[] 1. As a catalyst along with Cu(II) for the deamination of phenethylamines to phenyl substituted pyrroles.[] 2. Together with PEG 300, promoted efficient Suzuki-coupling of aryl chlorides with aryl boronic acids.[] 3. For small scale and high throughput uses, product is also available as ChemBeads (919853) (link product#)