Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 12069881 | HCID 12069881 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Phosphonium, ethyltriphenyl-, bromide (1:1) | HCID 73727 | — |
| Product | HCID 86759055 | HCID 86759055 | 25% |
Reaction Steps
Ethyl triphenylphosphonium bromide (0.98 g; 2.65 mmol) was added to benzene (15 ml). While the mixture was stirred under nitrogen atmosphere at room temperature, n-butyl lithium in n-hexane (1.56 M: 1.70 ml; 2.65 mmol) was added dropwise. The mixture was stirred for 5 minutes, and Compound 1 (0.50 g; 1.76 mmol) in benzene (5 ml) was added dropwise thereto, followed by heating under reflux for 3 hours. Subsequently, the mixture was left to cool to room temperature, and reaction was stopped by pouring the mixture into ice/water, followed by extraction with benzene (100 ml). The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=20:1), to thereby yield 0.13 g of the target compound (yield: 25.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586633B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-4b53d333af7149caa2c8a2067b60cb96 |
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| Source note | uspto-grants-2003_07 |
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