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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 250195Erstellt: 24. Oktober 2026

Sodium Hydroxide → [3-(5-Methoxy-benzofuran-2-yl)-3-phenyl-propyl]-methyl-amine

https://huagongshe.com/de/reaction/250195

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt5-MethoxybenzofuranHCID 25943—
EduktHCID 58088435HCID 58088435—
LösungsmittelMethanolHCID 887—
Produkt[3-(5-Methoxy-benzofuran-2-yl)-3-phenyl-propyl]-methyl-amineHCID 11623507—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

5-methoxybenzofuran (0.48 g) and trifluoro-acetic acid 3-[methyl-(2,2,2-trifluoro-acetyl)-amino]-1-phenyl-propyl ester (0.48 g) were mixed and heated in a sealed tube at 110° C. for 90 minutes. Upon cooling, the reaction mixture was taken up in methanol and treated with excess 1N sodium hydroxide solution, sufficient to form a strongly basic solution. After stirring for 20 minutes, the reaction mixture was concentrated at reduced pressure to remove the bulk of the methanol. The resulting mixture was partitioned between ethyl acetate and water. The layers were separated and the organic layer was evaporated to dryness. Purification by column chromatography (silica gel, dichloromethane (130):methanol (10):ammonium hydroxide (1)) followed by preparative tlc afforded [3-(5-Methoxy-benzofuran-2-yl)-3-phenyl-propyl]-methyl-amine (M+H=296) as the major component.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863305B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-8bfd3924d9a14e69914d03f9d7cc7dba
Quellennotizuspto-grants-2011_01