HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251530Generated: November 3, 2026
Hexane → 1-Cyclopentadienyl-1-(2,7-di-tert-butylfluorenyl)cyclohexane
https://huagongshe.com/reaction/1251530
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2,7-Di-tert-butylfluorene | HCID 4090082 | — |
| Reactant | Cyclohexylfulvene | HCID 22327799 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Cyclopentadienyl-1-(2,7-di-tert-butylfluorenyl)cyclohexane | HCID 131723104 | 67.9% |
Reaction Steps
To a THF (30 ml) solution including 5.0 g (18.6 mmol) of 2,7-di-tert-butylfluorene, a hexane solution (13.5 ml, 21.6 mmol) of n-butyllithium was added dropwise at −78° C. under nitrogen, followed by stirring at room temperature for 6 hours. Next, a THF (20 ml) solution including 3.42 g (23.4 mmol) of cyclohexylfulvene was added dropwise at 0° C. under a nitrogen atmosphere, followed by stirring at room temperature for 16 hours. The resultant reaction solution was decomposed with cold water, and then extracted with ether. The extract was dried over magnesium sulfate and then filtered, and the used solvent was removed from the filtrate under reduced pressure, thereby obtaining a solid. This solid was recrystallized from methanol to obtain 5.36 g of a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06342568B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-7c02aa446e3949f4a0b6f1a920c296a1 |
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| Source note | uspto-grants-2002_01 |
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