HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 427197Erstellt: 25. Oktober 2026
4-Hydroxybenzaldehyde → 4-(3-Trimethylsilanylpropyloxy)benzaldehyde
https://huagongshe.com/reaction/427197
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | (3-Chloropropyl)trimethylsilane | HCID 75362 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(3-Trimethylsilanylpropyloxy)benzaldehyde | HCID 21881562 | 86% |
Reaktionsschritte
3-chloropropyltrimethylsilane (33.14 g, 0.22 mol) was added dropwise over 10 minutes to a mixture of 4-hydroxybenzaldehyde (24.4 g, 0.2 mol) and potassium carbonate (30.4 g, 0.22 mol) in 150 ml of dry DMF maintained at 120° C. under nitrogen. The mixture was maintained for 2 hours, 30 minutes, at 120°-130° C. The reaction mixture was cooled and poured into ice-cold water. The aqueous phase was extracted 3 times with dichloromethane. The organic phases were dried over sodium sulfate and concentrated under vacuum. After distillation under vacuum (0.2 mmHg), 40.5 g (yield: 86%) of 4-(3-trimethylsilanylpropyloxy) benzaldehyde were obtained in the form of a colorless oil distilling at 110-114° C. and employed without further purification in the following step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06312673B2 |
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| Quelldatensatz | uspto-grants-2001_11 |
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| ORD ID | ord-78de7a58c1ca41efb0637ee822403093 |
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| Quellennotiz | uspto-grants-2001_11 |
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