Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Terephthalaldehyde | HCID 12173 | — |
| Edukt | Ethanol sodium ethoxide | HCID 23706232 | — |
| Edukt | 9-Decenoxybenzyltriphenylphosphonium bromide | HCID 86609565 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 9-Decenoxystilbene aldehyde | HCID 86609564 | 50% |
Reaktionsschritte
First, 23.07 g (0.039 M) of 9-decenoxybenzyltriphenylphosphonium bromide (compound (26)) prepared in Synthetic example 1-4 and 5.91 g of terephthalaldehyde (compound (12)) were dissolved in 315 mL of ethanol. The resulting solution was cooled to −2° C., and then 25.64 g of a sodium ethoxide ethanol solution (21 percent by weight, aldrich) was added dropwise at 0° C. or less. Aging was performed at a mixture temperature of 0° C. or less for 1.5 hours and then at a mixture temperature of 10° C. to 15° C. for 2 hours. After aging, 39 g of deionized water was added dropwise. Then, the precipitated crystals were filtrated and washed with 50 mL of 60% aqueous ethanol and 30 mL of ethanol, followed by drying. Thereby, 7.12 g of 9-decenoxystilbene aldehyde (compound (27)) was produced (yield: 50.0%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07422702B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-8dd330e147894c23aac825f85ed05457 |
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| Quellennotiz | uspto-grants-2008_09 |
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