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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 350081Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/350081

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTetrahydrofuranHCID 8028—
EduktSodium HydroxideHCID 14798—
EduktEthyl 3-[1-[6-(2-fluorobenzyloxy)-2-naphthylmethyl]-4-phenyl-3-pyrrolyl]propionateHCID 69422683—
LösungsmittelEthanolHCID 702—
Produkt3-[1-[6-(2-Fluorobenzyloxy)-2-naphthylmethyl]-4-phenyl-3-pyrrolyl]propionic acidHCID 6942174976,3%

Reaktionsschritte

A mixture of ethyl 3-[1-[6-(2-fluorobenzyloxy)-2-naphthylmethyl]-4-phenyl-3-pyrrolyl]propionate (401 mg), 1N aqueous sodium hydroxide solution (2 ml), tetrahydrofuran (4 ml) and ethanol (4 ml) was stirred at room temperature for 7 hours, and 1N hydrochloric acid (2 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-[6-(2-fluorobenzyloxy)-2-naphthylmethyl]-4-phenyl-3-pyrrolyl]propionic acid (289 mg, yield: 76%). This was recrystallized from ethanol-hexane. Melting point: 143–144° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179823B1
Quelldatensatzuspto-grants-2007_02
ORD IDord-433cdff2a37245fdb1bae7d4b18cb610
Quellennotizuspto-grants-2007_02