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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium BicarbonateHCID 516892—
Edukt3-(4-Methoxy-phenoxy)-propylamineHCID 3152109—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt3-(t-Butyldimethylsilyloxy)benzaldehydeHCID 11207111—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produktn-3-(4-Methoxyphenoxy)propyl-3-tert-butyldimethylsilyloxybenzylamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07183295B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-1f5970dd638c4c0a941f58a35a661d4a
Quellennotizuspto-grants-2007_02