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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | P-Chloroacetophenone | HCID 7467 | — |
| Edukt | Dimethyl oxalate | HCID 11120 | — |
| Edukt | Butyrate | HCID 104775 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Methyl 3-oxo-4-(4-chlorophenyl)butanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05643933 |
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| Quelldatensatz | uspto-grants-1997_07 |
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| ORD ID | ord-fc6349c0750e4c6fae39c6f3f62f6318 |
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| Quellennotiz | uspto-grants-1997_07 |
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