Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 11139790 | HCID 11139790 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15913958 | HCID 15913958 | — |
Reaction Steps
1.36 g, 5.26 mmol of 1,2-bis(2-indenyl)ethane, prepared as described in the above reported Synthesis 1(a), were dissolved in 25 mL THF and cooled to −10° C. 5.5 ml of a 1.6 M solution of BuLi in hexane (8.8 mmoles) were added and the resulting orange/brown solution was stirred for 2 hours, at room temperature. To the obtained ;mixture was added, by means of a cannula, a solution of 1.1 ml of EtI (7.1 mmol) in 10 ml THF, at −10° C. After 2 hours, the THF was removed under vacuum, and Et2O was added. The thus obtained ether solution was washed 3 times with a saturated solution of NaHCO3 and 3 times with a saturated aqueous solution of NaCl. After drying over MgSO4, 1.46 g of 1,2-bis(1-ethyl-2-indenyl)ethane was isolated, in the form of a yellow oil. 1H NMR and GC showed that it consisted of the three possible double bond isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06306791B2 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-8808ef5f89cd400bbcc9d29548c36377 |
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| Source note | uspto-grants-2001_10 |
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