BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)

BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Basic information
Product Name:BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)
Synonyms:[Pd(NCOC2H4CO)(PPh3)2Br];BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II);bromo(n-succinimidyl)bis(triphenylphosphine)palladium(ii);trans-Bromo(N-succinimidyl)bis(triphenylphosphine)palladium(II);trans-BroMo(N-succiniMidyl)bis(triphenylphosphine)palladiuM(II),97%;bromopalladium, pyrrolidin-1-ide-2,5-dione, triphenylphospho...;BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II)
CAS:251567-28-9
MF:C40H37BrNO2P2Pd
MW:812.01
EINECS:
Product Categories:
Mol File:251567-28-9.mol
BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Structure
BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Chemical Properties
Melting point 223-228 °C (dec.) (lit.)
Safety Information
WGK Germany 3
MSDS Information
BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Usage And Synthesis
Usestrans-Bromo(N-succinimidyl)bis(triphenylphosphine)palladium(II) may be used in the following processes:
  • As a catalyst for the preparation of 6-cyano-2-(3-fluoro-benzyl)-indole-1-carboxylic acid tert-butyl ester via Suzuki cross-coupling reaction between 1-boc-6-cyanoindole-2-boronic acid and 3-fluorobenzyl bromide. This method does not involve the use of strong bases or toxic reagents and also the use of this catalyst minimizes protodeboronation.
  • As a precatalyst for the Suzuki-Miyaura cross-coupling reaction between alkenyl tosylates and alkenyl MIDA boronates in the absence of phosphine ligands. For less activated alkenyl tosylate, the addition of tricyclohexylphosphine tetrafluoroborate improves the reactivity.
BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Preparation Products And Raw materials
Succinimide

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