HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 495108Erstellt: 24. Oktober 2026
3-(4-Methoxy-phenoxy)-propylamine → butyl (R)-2-(3-(((3-(4-methoxyphenoxy)propyl)amino)methyl)phenoxy)butanoate
https://huagongshe.com/de/reaction/495108
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3-(4-Methoxy-phenoxy)-propylamine | HCID 3152109 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | n-butyl (R)-2-(3-formylphenoxy)butyrate | HCID 11846216 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | butyl (R)-2-(3-(((3-(4-methoxyphenoxy)propyl)amino)methyl)phenoxy)butanoate | HCID 57552765 | — |
Reaktionsschritte
3-(4-Methoxyphenoxy)propylamine (34 mg) was dissolved in methanol (3 mL), and a solution (2 mL) of n-butyl (R)-2-(3-formylphenoxy)butyrate (50 mg) in methanol was added thereto under stirring at room temperature. The mixture was further stirred at 80° C. for 12 hours. Subsequently, an aqueous solution (0.5 mL) of sodium borohydride (7 mg) was added to the solution at room temperature, and the mixture was stirred for 30 minutes. The reaction solution was concentrated under reduced pressure, and chloroform was added to the concentrated product. The formed organic layer was washed with water. The washed organic layer was dried over sodium sulfate anhydrate, and concentrated under reduced pressure, to thereby yield 81 mg of a pale yellow, oily substance. The entirety of the substance was employed in the following reaction without any further treatment.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07538242B2 |
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| Quelldatensatz | uspto-grants-2009_05 |
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| ORD ID | ord-327652398a9a490d921bd1883f59e10a |
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| Quellennotiz | uspto-grants-2009_05 |
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