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CAS RN: 104439-77-2 | Product Number: H1322
1-Hydroxytetraphenylcylclopentadienyl(tetraphenyl-2,4-cyclopentadien-1-one)-μ-hydrotetracarbonyldiruthenium(II)
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Purity:
Synonyms:
- Shvo's Catalyst
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 100MG |
NT$3,760
|
5 | 12 | Contact Us |
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| Product Number | H1322 |
| Molecular Formula / Molecular Weight | C__6__2H__4__2O__6Ru__2 = 1,085.15 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Air Sensitive,Moisture Sensitive |
| Packaging and Container | 100MG-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 104439-77-2 |
| PubChem Substance ID | 125308084 |
| Merck Index (14) | 8483 |
| MDL Number | MFCD03840556 |
Specifications
| Appearance | Light yellow to Brown powder to crystal |
| Elemental analysis(Carbon) | 67.0 to 71.0 % |
Properties (reference)
| Melting Point | 227 °C |
GHS
Related Laws:
Transport Information:
| H.S.code* | 2843.90-000 |
Application
Reviews
References
- Shvo's diruthenium complex: a robust catalyst
- Discovery, Applications, and Catalytic Mechanisms of Shvo’s Catalyst
Application
Anti-Markovnikov Hydration of Vinylarenes via Triple Relay Catalysis
Typical procedure (R = H): PdCl2(CH3CN)2 (10.4 mg), Shvo’s catalyst (43.6 mg), CuCl2 (10.8 mg) and 1,4-benzoquinone (43.2 mg) are weighed into a 20 mL vial under a nitrogen atmosphere, followed by the addition of i-PrOH (2 mL) and t-BuOH (4 mL). Styrene (41.7 mg) is added to the mixture followed by addition of H2O (8.1 µL). After the resulting mixture is stirred at 85 °C for 6 h, it is diluted with pentane (6 mL) and filtered through a plug of silica gel followed by flushing with ethyl acetate (6 mL). The solvent is removed under vacuum, and the residue is purified by silica gel flash chromatography to give 2-phenylethyl alcohol (41 mg, 87 % yield).
References
Application
Synthesis of Aromatic Amines under Catalytic Transfer Hydrogenation Conditions
Typical procedure (entry 1): In a pressure tube under an argon atmosphere, the Shvo’s catalyst (22 mg), p-toluidine (429 mg), and hexylamine (202 mg) are dissolved in tert-amyl alcohol (0.5 ml). The pressure tube is fitted with a polytetrafluoroethylene cap and heated at 150 °C for 24 h in an oil bath. The solvent is removed in vacuo, and the crude product is purified by column chromatography (eluent: pentane/ethyl acetate) to give N-hexyl-4-methylaniline as colorless crystals (374 mg, 98 %).
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