Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Tert-butylcyclopentadiene | HCID 633714 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Butyl-6,6-dimethylfulvene | HCID 17896375 | 92% |
Reaction Steps
A mixture of t-butylcyclopentadiene (15 g, 123 mmol), acetone (9.0 mL, 135.2 mmol), pyrrolidine (11.7 mL, 135.3 mmol) and methanol (100 mL) was stirred at 0° C., for 30 minutes, and then at room temperature overnight. The reaction mixture was quenched with acetic acid (7.38 g) and with water (100 mL) at 0° C. The mixture was extracted with Et2O (3×200 mL); the organic layers were combined, washed with a saturated solution of NaHCO3, dried over anhydrous magnesium sulphate, filtered and finally concentrated, thus yielding 2-butyl-6,6-dimethylfulvene in the form of a yellow liquid (18.24 g, 92% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06162937 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-17096a16e3fa42ea8470d07a22a0de7e |
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| Source note | uspto-grants-2000_12 |
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