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CAS RN: 13965-03-2 | Product Number: B1667
Bis(triphenylphosphine)palladium(II) Dichloride
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Purity: >98.0%(T)
Synonyms:
- Dichlorobis(triphenylphosphine)palladium(II)
Product Documents:
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| 1G |
$59.00
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0 | ≥100 | It can be shipped in about 2-3 business days after ordering | |
| 5G |
$167.00
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≥40 | ≥100 | It can be shipped in about 5-6 months after ordering | |
| 25G |
$589.00
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≥60 | ≥100 | It can be shipped in about 5-6 months after ordering |
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| Product Number | B1667 |
| Purity / Analysis Method | >98.0%(T) |
| Molecular Formula / Molecular Weight | C__3__6H__3__0Cl__2P__2Pd = 701.90 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Refrigerated (0-10°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Moisture Sensitive,Heat Sensitive |
| Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 13965-03-2 |
| Reaxys Registry Number | 13172189 |
| PubChem Substance ID | 87564568 |
| SDBS (AIST Spectral DB) | 27199 |
| MDL Number | MFCD00009593 |
Specifications
| Appearance | Light yellow to Brown powder to crystal |
| Purity(Chelometric Titration) | min. 98.0 % |
| NMR | confirm to structure |
Properties (reference)
GHS
Related Laws:
Transport Information:
| H.S.code* | 2843.90-000 |
Application
TCI Practical Example: Sonogashira Cross Coupling
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Used Chemicals
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Procedure
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To a two-necked flask was charged with iodobenzene (1.09 mL, 9.80 mmol, 1.0 equiv.), ethynylbenzene (1.18 mL, 10.7 mmol, 1.1 equiv.), bis(triphenylphosphine)palladium(II) dichloride (137 mg, 0.195 mmol 2.0 mol%), copper(I) iodide (40 mg, 0.210 mmol, 2.1 mol%), tetrahydrofuran anhydrous (40 mL), triethylamine (1.90 mL, 14.7 mmol, 1.5 equiv.) under nitrogen atmosphere. The mixture was stirred at room temperature for 1.5 h. The reaction mixture was quenched with water (20 mL). The organic layer was washed with brine (10 mL), dried over Na2SO4 and then concentrated under reduce pressure. The crude was purified by column chromatography on silica gel (hexane) to afford diphenylacetylene as a white powder (1.70 g, 97 %).
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Experimenter’s Comments
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The reaction mixture was monitored by GC.
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Analytical Data
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Diphenylacetylene
1H NMR (400 MHz, CDCl3); δ 7.51-7.54 (m, 4H), 7.31-7.35 (m, 6H).
13C NMR (101 MHz, CDCl3); δ 131.6, 128.3, 128.2, 123.2, 89.3.
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Other References
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- A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines
Application
One-pot Procedure for the Synthesis of Unsymmetrical Diarylalkynes
References
- One-Pot Procedure for the Synthesis of Unsymmetrical Diarylalkynes
PubMed Literature
Articles/Brochures
TCIMAIL
[TCI Practical Example] Sonogashira Cross Coupling with PdCl2(PPh3)2 as a Catalyst[Research Articles] One-pot Procedure for the Synthesis of Unsymmetrical Diarylalkynes
Product Documents (Note: Some products will not have analytical charts available.)
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Specifications
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