HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23710Erstellt: 23. Oktober 2026
Imidazole → 4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehyde
https://huagongshe.com/de/reaction/23710
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Imidazole | HCID 795 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Edukt | Benzaldehyde, 4-(2-hydroxyethoxy)- | HCID 89178 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehyde | HCID 57956101 | 49,9% |
Reaktionsschritte
To 4-(2-hydroxyethoxy)benzaldehyde (commercial, 0.5 g, 3 mmol) dissolved in DMF (10 mL) is added imidazole (0.4 g, 6 mmol) and tert-butyldimethylsilylchloride (0.53 g, 3.5 mmol). Reaction mixture is stirred for 20 h. at room temperature. TLC analysis (hexane:ethyl acetate,7:3) shows small amounts of unreacted starting material. Additional tert-butyldimethylsilylchloride (0.25 g, 1 mmol) is added and stirring continued for 16 h. The reaction is quenched with saturated aqueous ammonium chloride (20 mL) and diluted further with ethyl ether (20 mL). Aqueous layer is separated and extracted thrice with ether (10 mL). Combined organics dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue is purified by flash chromatography on silica gel using a gradient of 2% to 5% ethyl acetate in hexanes to provide 0.42 g of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06852731B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-80c3f0ea60a240ea855be153730b5b6d |
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| Quellennotiz | uspto-grants-2005_02 |
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