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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: | C40H34BrNO2P2Pd | | MW: | 0 | | EINECS: | | Product Categories: | | Mol File: | 251567-28-9.mol |
| BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Chemical Properties |
| Melting point | 223-228 °C (dec.) (lit.) |
| 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.
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| BROMOBIS(PH3P)(N-SUCCINIMIDE)PD(II) Preparation Products And Raw materials |
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