Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperonal | HCID 8438 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 23110274 | HCID 23110274 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68843936 | HCID 68843936 | 178.7% |
Reaction Steps
A suspension of 2,7-bis(diethylphosphonatomethyl)-9,9-dipropylfluorene (4) (2.70 g, 5 mmol), 3,4-methylenedioxybenzaldehyde (7) (1.60 g, 11 mmol) and potassium hydroxide (0.85 g, 15 mmol) in THF (30 mL) and DMSO (1 mL) was heated at 70° C. for 7 hours. The suspension was diluted with Ethanol (50 mL) and the solvent removed under vacuum. The product was purified by refluxing in Methanol followed by filtration. After drying, (II-5) was obtained as a pale yellow powder (1.95 g, 72%). The UV/VIS spectrum of (II-5) in methyl ethyl ketone (MEK) has two maxima at 382 nm and at 401 nm with a molar extinction coefficient of 79099 Mol−1 cm−1 and 63911 Mol−1 cm−1 respectively. Under UV irradiation (II-5) shows a strong blue fluorescence. The 1H-NMR data in CDCl3 are summarized in table 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439537B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-0d25027fb03c4910bdf09e2b4b824317 |
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| Source note | uspto-grants-2008_10 |
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