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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 547147Erstellt: 25. Oktober 2026

Sodium Hydroxide → (4'-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-4-methoxy-biphenyl-3-yl)-acetic Acid

https://huagongshe.com/reaction/547147

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktAmmonium ChlorideHCID 25517—
Edukt(4'-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-4-methoxy-biphenyl-3-yl)-acetic Acid Methyl EsterHCID 57709162—
LösungsmittelMeOH tetrahydrofuranHCID 21899815—
Produkt(4'-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-4-methoxy-biphenyl-3-yl)-acetic AcidHCID 5770911487,3%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A 1 N sodium hydroxide aqueous solution (0.200 mL, 0.200 mmol) was added to a solution of (4′-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-pentenyl)-3-methyl-phenyl]-propyl}-4-methoxy-biphenyl-3-yl)-acetic acid methyl ester (Example 180-(2); 35.2 mg, 0.067 mmol) in methanol-tetrahydrofuran (1:1, 4 mL), and the mixture was stirred at 60° C. for two hours. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution, followed by extraction with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (chloroform:methanol=10:1) to give the target compound as a colorless oil (30.1 mg, 87%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07935688B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-b4e08a6db266429eb56691c6722f44d4
Quellennotizuspto-grants-2011_05