Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Fluorene | HCID 6853 | — |
| Reactant | 1,3-Cyclopentadiene, 5-(1-methylethylidene)- | HCID 137467 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 129845837 | HCID 129845837 | 68.6% |
Reaction Steps
To 200 ml of THF and 16.5 g of fluorene cooled to a temperature of -50° C. or lower in a 500-ml flask thoroughly purged with nitrogen was added 67 ml of a dil. methyllithium diethyl ether solution (1.4 M) dropwise over 30 minutes. The mixture was warmed gradually to room temperature and subjected to reaction for 3 hours. The reaction mixture was cooled back to a temperature of -50° C. or lower and 10 g of 6,6-dimethylfulvene was added dropwise over 30 minutes. After the addition was completed, the solution was warmed slowly to room temperature and subjected to reaction for 2 days. The reaction was terminated by the addition of 60 ml of H2O, and the ether layer was separated and dehydrated over anhydrous MgSO4. Drying ether by evaporation, gave 17.6 g of 2-cyclopentadienyl-2-fluorenylpropane as crude crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05225501 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-85388c2674a34fdfa6b5689de3b6eb55 |
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| Source note | uspto-grants-1993_07 |
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