HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263644Generated: October 26, 2026
P-Chloroacetophenone → Methyl 3-oxo-4-(4-chlorophenyl)butanoate
https://huagongshe.com/reaction/263644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Chloroacetophenone | HCID 7467 | — |
| Reactant | Dimethyl oxalate | HCID 11120 | — |
| Reactant | Butyrate | HCID 104775 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-oxo-4-(4-chlorophenyl)butanoate | HCID 22246215 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05643933 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-fc6349c0750e4c6fae39c6f3f62f6318 |
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| Source note | uspto-grants-1997_07 |
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