Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 263644Erstellt: 27. Oktober 2026

P-Chloroacetophenone → Methyl 3-oxo-4-(4-chlorophenyl)butanoate

https://huagongshe.com/reaction/263644

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktP-ChloroacetophenoneHCID 7467—
EduktDimethyl oxalateHCID 11120—
EduktButyrateHCID 104775—
EduktSodiumHCID 5360545—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
ProduktMethyl 3-oxo-4-(4-chlorophenyl)butanoateHCID 22246215—

Reaktionsschritte

Dimethyl oxalate (15.27 g, 0,129 mol), and 4'-chloroacetophenone (20.0 g, 0.129 mol) were added to methanol (300 mL). Sodium methoxide (25 wt. % in methanol, 70 mL) was added dropwise over about 0.5 hour. The reaction was stirred at room temperature for 16 hours, whereupon the sodium salt of the butanoate precipitated from solution. The mixture was treated with 70 mL of conc. HCl and the white suspension was stirred vigorously at room temperature for 1 hour. The suspension was cooled to 0° C. and held for 0.5 hour. The solid was filtered, and the filter cake was washed with cold water (100 mL). After drying in vacuo, methyl 4-[4-(chloro)phenyl]-3-ketobutyrate was obtained (16.94 g, 54.4%) as the enol: 1H NMR (CDCl3 /300 MHz) 8 7.94 (d, J=8.66 Hz, 2H), 7.48 (d, J=8.66 Hz, 2H), 7.04 (s, 1H), 3.95 (s, 3H), 3.48 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05643933
Quelldatensatzuspto-grants-1997_07
ORD IDord-fc6349c0750e4c6fae39c6f3f62f6318
Quellennotizuspto-grants-1997_07