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

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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
Mol File:
251567-28-9.mol
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BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Chemical Properties

Melting point:
223-228 °C (dec.) (lit.)
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Safety Information

WGK Germany 
3
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BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Usage And Synthesis

Uses

trans-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)Supplier

Energy Chemical
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Beijing Guofang Dingsheng Technology Co., Ltd.
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Sigma-Aldrich
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021-61415566 800-8193336
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orderCN@merckgroup.com
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