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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2987Erstellt: 24. Oktober 2026

Acetone → 2-(4-Acetamidophenoxy)-2-methylpropanoic acid

https://huagongshe.com/de/reaction/2987

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktAcetaminophenHCID 1983—
EduktChloroformHCID 6212—
EduktSodium HydroxideHCID 14798—
Edukt2-(4-Aminophenoxy)-2-methylpropanoic acidHCID 2774958—
Produkt2-(4-Acetamidophenoxy)-2-methylpropanoic acidHCID 1487985560%

Reaktionsschritte

FIG. 2A illustrates a reaction scheme for preparing 2-(4-aminophenoxy)-2-methyl propionic acid, a compound that is useful as a precursor in the preparation of Group I compounds. In accordance with the scheme of FIG. 2A, 8 grams (g) (0.2 mol) of pulverized sodium hydroxide is added to a suspension of 5.28 g (0.035 mol) of p-acetamidophenol in 23 ml (0.4 mol) of acetone. The reaction mixture is stirred at room temperature for 1/2 hour. Subsequently, 3.58 g (0.03 mol) of chloroform is added dropwise over the course of 30 minutes. The reaction mixture is stirred overnight at room temperature and acetone is removed under vacuum. The residue is dissolved in water (10 ml), followed by acidification with 37% hydrochloric acid (HCl) to produce a pale yellow precipitate of 2-(4-acetaminophenoxy)-2-methyl propionic acid (5 g, 60% yield), crystallized from methanol, mp 69°-71° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731454
Quelldatensatzuspto-grants-1998_03
ORD IDord-8d4bf2d31e824543ac5f1049cd6477c4
Quellennotizuspto-grants-1998_03