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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 350052Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-[1-[4-(2-Methyl-3-pyridylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]propionic acid

https://huagongshe.com/de/reaction/350052

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTetrahydrofuranHCID 8028—
EduktSodium HydroxideHCID 14798—
EduktEthyl 3-[1-[4-(2-methyl-3-pyridylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]propionateHCID 69423888—
LösungsmittelEthanolHCID 702—
Produkt3-[1-[4-(2-Methyl-3-pyridylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]propionic acidHCID 6942298287,3%

Reaktionsschritte

A mixture of ethyl 3-[1-[4-(2-methy-3-pyridylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]propionate (568 mg), 1N aqueous sodium hydroxide solution (3 ml), tetrahydrofuran (6 ml), and ethanol (6 ml) was stirred at room temperature for 4 hours, and 1N hydrochloric acid (3 ml) was added to the mixture, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), then concentrated. The colorless crystals obtained were collected by filtration to yield 3-[1-[4-(2-methyl-3-pyridylmethoxy)benzyl]-4-phenyl-3-pyrrolyl]propionic acid (465 mg, yield: 87%). This was recrystallized from ethyl acetate-hexane. Melting point: 158–159° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179823B1
Quelldatensatzuspto-grants-2007_02
ORD IDord-a1d29a95cb484d83908bf18e6ebcce29
Quellennotizuspto-grants-2007_02