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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 322879Erstellt: 26. Oktober 2026

Potassium Iodide → ethyl (RS)-4-(2-acetyl-5-benzyloxy-phenoxy)-4-phenylbutanoate

https://huagongshe.com/reaction/322879

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt4'-Benzyloxy-2'-hydroxyacetophenoneHCID 309257—
EduktEthyl 4-chloro-4-phenylbutanoateHCID 12847348—
LösungsmittelDimethylformamideHCID 6228—
Produktethyl (RS)-4-(2-acetyl-5-benzyloxy-phenoxy)-4-phenylbutanoateHCID 2320430734,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 4-benzyloxy-2-hydroxyaceto-phenone (1.2 g), ethyl (RS)-4-chloro-4-phenyl-butanoate (1.21 g), potassium carbonate (760 mg), potassium iodide (35 mg) and dimethylformamide (30 mL) is stirred at 100° C. for 8 hours. It is evaporated to dryness and the resulting residue is partitioned between ethyl acetate (200 mL) and water (200 mL). The organic layer is dried over magnesium sulphate, filtered and concentrated in vacuo. Flash chromatography of the resulting oil, eluting with 15-30% ethyl acetate/hexane, affords ethyl (RS)-4-(2-acetyl-5-benzyloxy-phenoxy)-4-phenylbutanoate (0.73 g), in the form of a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211234B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-38a7180b845244e4becca23853d94f6e
Quellennotizuspto-grants-2001_04