| Identification | Back Directory | [Name]
Methanesulfonato(diadamantyl-n-butylphosphino)-2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct, min. 95% [cataCXium(R) A Palladacycle Gen. 3] | [CAS]
1651823-59-4 | [Synonyms]
Methanesulfonato(diadamantyl-n-butylphosphino)-2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct, min. 95% [cataCXium(R) A Palladacycle Gen. 3] | [Molecular Formula]
C37H52NO3PPdS | [MDL Number]
MFCD28144563 | [MOL File]
1651823-59-4.mol | [Molecular Weight]
728.28 |
| Questions And Answer | Back Directory | [Synthesis]
In a dry reaction flask, the biphenyl palladium dimer precursor compound (277 mg) was added, followed by adamantane butylphosphine ligand (269 mg). The flask was then sealed, evacuated with argon gas, and backfilled three times. Degassed acetone (3 mL) was added to the flask via a syringe, and the resulting reaction mixture was stirred overnight at room temperature. After the reaction was complete, the reaction mixture was filtered under vacuum, and the precipitate was collected. The precipitate was washed sequentially with acetone and pentane to obtain the target catalyst. Note that this catalyst is sensitive to oxygen; post-processing should be rapid to avoid direct contact with air as much as possible. | [Reaction]
Precatalyst for the palladium-catalyzed cross-coupling of cesium trifluoroborate salts with aryl halides.
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| Chemical Properties | Back Directory | [Melting point ]
196-241 °C (decomposition) | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [form ]
Powder | [color ]
off-white | [InChIKey]
VIYNMTFDXQNMCC-UHFFFAOYSA-N | [SMILES]
P(C12CC3CC(CC(C3)C1)C2)(C12CC3CC(CC(C3)C1)C2)([Pd+2]1(NC2=CC=CC=C2C2=CC=CC=[C-]12)[O-]S(=O)(=O)C)CCCC |
| Hazard Information | Back Directory | [Uses]
cataCXium? A Pd G3 is a Buchwald third generation precatalyst that can be used in:
- Direct ortho-arylation of pyridinecarboxylic acids.
- Catalyzing Suzuki–Miyaura cross-coupling in the synthesis of 1-heteroaryl-3-azabicyclo[3.1.0]hexanes.
- Palladium-catalyzed carbonylative carboperfluoroalkylation of alkynes.
- Suzuki–Miyaura coupling reaction of geminal bis(boryl)cyclopropanes in the synthesis of various gem-disubstituted cyclopropanes.
| [reaction suitability]
reagent type: catalyst reaction type: Cross Couplings |
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| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
| Company Name: |
Jia Xing Isenchem Co.,Ltd
|
| Telephone: |
0573-85285100 18627885956 |
| Website: |
https://www.chemicalbook.com/ShowSupplierProductsList14265/0_EN.htm |
| Company Name: |
T&W GROUP
|
| Telephone: |
021-61551611 13296011611 |
| Website: |
www.trustwe.com/ |
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