HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24377Erstellt: 23. Oktober 2026
Triphenylphosphine → 3,5-Diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehyde
https://huagongshe.com/de/reaction/24377
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | 2-Morpholinoethanol | HCID 61163 | — |
| Edukt | 4-Hydroxy-3,5-bis(isopropyl)benzaldehyde | HCID 82712 | — |
| Edukt | Diethyl azodicarboxylate | HCID 5462977 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3,5-Diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehyde | HCID 22571130 | 14,4% |
Reaktionsschritte
Triphenylphosphine (5.14 g, 19.58 mmol) was added to a solution of 3,5-diisopropyl-4-hydroxybenzaldehyde (4 g, 19.58 mmol) in tetrahydrofuran (40 ml) followed by addition of 2-hydroxyethylmorpholine (2.57 g, 19.58 mmol) and then the dropwise addition of diethylazodicarboxylate (3.41 g, 19.58 mmol). The mixture was stirred at room temperature for 12 hours. The reaction was concentrated under reduced pressure and partitioned between 2N hydrochloric acid (200 ml) and ethyl acetate (150 ml). The aqueous layer was extracted with ethyl acetate (2×150ml), basified to pH 9 with solid sodium bicarbonate and extracted with ethyl acetate (3×150 ml). The organic layers were combined, dried over magnesium sulfate and concentrated to afford 900 mg (14%) of 3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehyde as a yellowish oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06855730B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-0b39b6e87327452e9407713dc876b76e |
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| Quellennotiz | uspto-grants-2005_02 |
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