HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 350840Erstellt: 26. Oktober 2026
Acetic Acid → n-3-(4-Methoxyphenoxy)propyl-3-tert-butyldimethylsilyloxybenzylamine
https://huagongshe.com/reaction/350840
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 3-(4-Methoxy-phenoxy)-propylamine | HCID 3152109 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Edukt | 3-(t-Butyldimethylsilyloxy)benzaldehyde | HCID 11207111 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | n-3-(4-Methoxyphenoxy)propyl-3-tert-butyldimethylsilyloxybenzylamine | HCID 21949684 | — |
Reaktionsschritte
3-tert-Butyldimethylsilyloxybenzaldehyde (1.5 g, 6.34 mmol) was dissolved in 1,2-dichloroethane (10.0 mL). Subsequently, 3-(4-methoxyphenoxy)propylamine (1.5 g, 8.25 mmol) was added thereto, and the resultant mixture was stirred for 20 minutes. At room temperature, sodium triacetoxyborohydride (1.75 g, 8.25 mmol) and acetic acid (495 mg, 8.25 mmol) were added thereto, and the mixture was stirred overnight. A saturated aqueous sodium hydrogencarbonate solution was added thereto. The reaction mixture was extracted with chloroform, and the organic layer was washed with brine. The resultant mixture was subjected to drying over anhydrous sodium sulfate, concentration under reduced pressure, and purification by silica gel chromatography (chloroform/methanol=50/1), whereby the target compound was obtained (1.9 g, 78%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07183295B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-1f5970dd638c4c0a941f58a35a661d4a |
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| Quellennotiz | uspto-grants-2007_02 |
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