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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1464518Erstellt: 25. Oktober 2026

Hydrochloric Acid → 6-Ethoxy-6-(4-methoxyphenyl)hexanoic acid

https://huagongshe.com/reaction/1464518

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolHCID 702—
EduktWaterHCID 962—
EduktEthyl 6-(4-methoxyphenyl)-6-oxohexanoateHCID 15098222—
EduktHCID 178418435HCID 178418435—
Produkt6-Ethoxy-6-(4-methoxyphenyl)hexanoic acidHCID 19088060—

Reaktionsschritte

A solution of ethyl 5-(4-methoxybenzoyl)pentanoate (50 g, 0.19 mole) in ethanol (500 ml) was cooled with ice, and sodium boron hydride (10 g) was added gradually to the solution. After the reaction was allowed to proceed for 1 hour, water (200 ml) and 2N hydrochloric acid (50 ml) were added to the reaction solution, followed by concentration under reduced pressure. The resulting residue was dissolved in ethyl acetate, and the organic layer was washed with water, dried and concentrated under reduced pressure. Methanol (300 ml), water (100 ml) and sodium hydroxide (40 g) were added to the resulting residue, followed by stirring for 2 hours, and the methanol was removed under reduced pressure. The water layer was washed with isopropyl ether and then adjusted to pH 4.0 with hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was washed with water, dried and concentrated under reduced pressure, and the residue was chromatographed on a silica gel column, followed by elution with isopropyl ether-ethyl acetate (1:1) to give firstly 6-ethoxy-6-(4-methoxyphenyl)hexanoic acid (21 g) and then 6-hydroxy-6-(4-methoxyphenyl)hexanoic acid (20 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05304658
Quelldatensatzuspto-grants-1994_04
ORD IDord-bb3b050121174f6abed579d2c4540a76
Quellennotizuspto-grants-1994_04