HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913593Generated: October 26, 2026
Fluorene → 2-(3-Tert-butyl-5-methylcyclopentadienyl)-2-fluorenylpropane
https://huagongshe.com/reaction/1913593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Fluorene | HCID 6853 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1,6,6-Trimethyl-3-tert-butyl-fulvene | HCID 2762761 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Tert-butyl-5-methylcyclopentadienyl)-2-fluorenylpropane | HCID 131725120 | 18.2% |
Reaction Steps
In a nitrogen atmosphere, a hexane solution of n-butyllithium (40 ml, 61.6 mmol) was added dropwise to a solution of fluorene (10.1 g, 60.8 mmol) in THF (300 ml) with ice cooling. The mixture was stirred at room temperature for 5 hours (resulting in a dark brown solution). The solution was ice cooled again, and a solution of 3-tert-butyl-1,6,6-trimethylfulvene (11.7 g, 66.5 mmol) in THF (300 ml) was added thereto dropwise in a nitrogen atmosphere. The reaction solution was stirred at room temperature for 14 hours. The resultant brown solution was ice cooled, and water (200 ml) was added. The obtained solution was extracted with diethyl ether. Then the organic phase was separated therefrom, and dried over magnesium sulfate. The organic phase was filtered, and the solvent was removed from the filtrate under reduced pressure, resulting in an orange-brown oil. The oil was purified by silica gel column chromatography (developing solvent: hexane) to give 3.8 g of a yellow oil. The analytical data are given below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609769B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-50903bc50da143429947ac75ec4aebfe |
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| Source note | uspto-grants-2013_12 |
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