RuPhos Pd G3

RuPhos Pd G3 Basic information
Reaction
Product Name:RuPhos Pd G3
Synonyms:Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-aMino-1,1'-biphenyl-2-yl)palladiuM(II), Min. 98% [RuPhos Palladacycle];Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-aMino-1,1'-biphenyl-2-yl)palladiuM(II), Min. 98%;RuPhos Pd G3 95%;Methanesulfonato(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II);(2-Dicyclohexylphosphino-2′,6′-diisopropoxy-1,1′-biphenyl)[2-(2′-amino-1,1′-biphenyl)]palladium(II) methanesulfonate;RuPhos Pd G3;RuPhos-G3-Palladacycle;RuPhos-Pd-G3
CAS:1445085-77-7
MF:C43H57NO5PPdS-
MW:837.375141
EINECS:
Product Categories:Buchwald Ligands&Precatalysts;Buchwald Precatalysts Series;Pd
Mol File:1445085-77-7.mol
RuPhos Pd G3 Structure
RuPhos Pd G3 Chemical Properties
Melting point 188-196°C (decomposition)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form Powder
color white
CAS DataBase Reference1445085-77-7
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-52/53
Safety Statements 26-61
WGK Germany 3
MSDS Information
RuPhos Pd G3 Usage And Synthesis
Reaction
  1. Palladium catalyst used for facile, C-N cross-coupling reactions.
  2. A practical synthesis of indoles via a Pd-catalyzed C-N ring formation.
Reactions of 1445085-77-7
UsesRuPhos Pd G3 can be used as a pre-catalyst in the following protocols:
  • Palladium-catalyzed Suzuki coupling of 5-p-toluenesulfonyltetrazoles with arylboronic acids to synthesize 1,5-disubstituted tetrazoles.
  • Suzuki-Miyaura catalyst-transfer polycondensation (SCTP) of 3-alkylthiophenes in the presence of N-methylimidodiacetic (MIDA)-boronate monomers.
  • Suzuki-Miyaura-cross-coupling of aminothiophenes.

General DescriptionRuPhos Pd G3 is a third generation (G3) Buchwald precatalyst that can be used in cross-coupling reactions for the formation of C-C, C–N, C–O, C–F, C–CF3, and C–S bonds. It is air-, moisture-, and thermally-stable and is highly soluble in a wide range of common organic solvents. Some of its unique features include lower catalyst loadings, shorter reaction time, efficient formation of the active catalytic species and accurate control of ligand: palladium ratio.
XPhos Pd G1 tBuXPhos Pd G1 RuPhos Pd G2 SPhos Pd G1, Methyl t-Butyl Ether Adduct SPhos Pd G3 t-BuBrettPhos Palladacycle Gen. 3 RuPhos Palladacycle Gen. 4 t-BuXphos Palladacycle Gen. 4 Palladacycle Gen. 3 BrettPhosPalladacycle SPhos Pd G2 RuPhos Pd G1 Methyl t--Butyl Ether Adduct XPhos Pd G2 BrettPhos Pd G3 Xantphos Pd G3 XPhos Pd G4 SPhos Palladacycle Gen. 4 XPhos Pd G3

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