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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 350083Erstellt: 25. Oktober 2026

Hydrochloric Acid → 3-[4-Phenyl-1-[6-(3-pyridylmethoxy)-2-naphthylmethyl]-3-pyrrolyl]propionic acid

https://huagongshe.com/reaction/350083

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTetrahydrofuranHCID 8028—
EduktSodium HydroxideHCID 14798—
EduktEthyl 3-[4-phenyl-1-[6-(3-pyridylmethoxy)-2-naphthylmethyl]-3-pyrrolyl]propionateHCID 23024809—
LösungsmittelEthanolHCID 702—
Produkt3-[4-Phenyl-1-[6-(3-pyridylmethoxy)-2-naphthylmethyl]-3-pyrrolyl]propionic acidHCID 6942391984,5%

Reaktionsschritte

A mixture of ethyl 3-[4-phenyl-1-[6-(3-pyridylmethoxy)-2-naphthylmethyl]-3-pyrrolyl]propionate (638 mg), 1N aqueous sodium hydroxide solution (2.5 ml), tetrahydrofuran (5 ml) and ethanol (5 ml) was stirred at room temperature overnight, and 1N hydrochloric acid (2.5 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 obtain 3-[4-phenyl-1-[6-(3-pyridylmethoxy)-2-naphthylmethyl]-3-pyrrolyl]propionic acid (508 mg, yield: 84%). This was recrystallized from ethanol. Melting point: 158–159° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179823B1
Quelldatensatzuspto-grants-2007_02
ORD IDord-9e87b406141241c2b94573b3b14c17ea
Quellennotizuspto-grants-2007_02