Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 2,6-Diphenyl-4H-pyran-4-one | HCID 283227 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20203945 | HCID 20203945 | 45% |
Reaction Steps
A 1.7M hexane solution (3.5 ml) containing 6 mmol of n-butyl lithium was added dropwise to 10 ml of an anhydrous tetrahydrofuran solution containing 1.24 g (5 mmol) of 2,6-diphenyl-γ-pyrone which was cooled to -20° C. One hour later, the reaction mixture was poured into 50 ml of a 6 wt% aqueous solution of perchloric acid. The precipitated solid was collected by filtration, dissolved in a small amount of methylene chloride and reprecipitated in diethyl ether. The precipitated yellow solid was separated by filtration and dried to obtain 0.88 g (yield: 45%) of 2,6-diphenyl-3-n-propylpyrylium perchlorate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663260 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-7db78350b34b4156acf78f2663d9a7ad |
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| Source note | uspto-grants-1987_05 |
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