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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 548571Erstellt: 25. Oktober 2026

(4-{3-[3-Bromo-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-2-methyl-phenoxy)-acetic acid methyl ester → (4-{3-[3-Bromo-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-2-methylphenoxy)-acetic acid

https://huagongshe.com/reaction/548571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-{3-[3-Bromo-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-2-methyl-phenoxy)-acetic acid methyl esterHCID 67159034—
LösungsmittelEthanolHCID 702—
LösungsmittelSodium HydroxideHCID 14798—
Produkt(4-{3-[3-Bromo-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-2-methylphenoxy)-acetic acidHCID 24752743—

Reaktionsschritte

A solution of (4-{3-[3-bromo-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-2-methyl-phenoxy)-acetic acid methyl ester (94 mg, 0.169 mmol) in ethanol (5 ml) and 1N NaOH (0.5 ml) was stirred at 75° C. for 30 min. The reaction mixture was evaporated and the residue dissolved in water (2 ml). Aqueous 1N HCl (0.6 ml) was added and the mixture was extracted with methylene chloride (3×15 ml). The combined organic phases were dried and evaporated to give the title compound in 79 mg (86%) yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943612B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-c7c46ac3bd344538b62c47b77f5a88c4
Quellennotizuspto-grants-2011_05