Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178420581 | HCID 178420581 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178438233 | HCID 178438233 | — |
Reaction Steps
To a nitrogen-replaced flask, 5.0 mL of a hexane solution containing n-butyllithium (concentration: 2.6 mol/L) was placed and cooled to −78° C. After 1.74 g of bis(cyclopentadienyl)ruthenium was added, 50 mL of tetrahydrofuran was added dropwise over one hour to react them. The reaction solution was allowed to stand for 2 hours to return the temperature to room temperature and thereafter a reaction was performed for 24 hours. The reaction solution was again cooled to −78° C., 9.81 g of ethyl bromide was added dropwise over one hour to react them, allowed to stand for 2 hours to room temperature, and the reaction was performed for 24 hours. After completion of the reaction, 100 mL of water was added and bis(ethylcyclopentadienyl)ruthenium was extracted with hexane and then hexane was evaporated from the extraction solvent to obtain 2.0 g of bis(ethylcyclopentadienyl) ruthenium.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07002032B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-79281d19b0904455a1a8dd4daa48da03 |
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| Source note | uspto-grants-2006_02 |
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