HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356765Generated: October 30, 2026
Water → Ethyl 4-(4-chloro-3-fluorophenyl)-4-oxobutanoate
https://huagongshe.com/reaction/2356765
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 4-Chloro-3-Fluorobenzaldehyde | HCID 2724985 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-(4-chloro-3-fluorophenyl)-4-oxobutanoate | HCID 24727751 | — |
Reaction Steps
Under argon atmosphere, to a solution of 4-chloro-3-fluoro-benzaldehyde (10 g) in N,N-dimethylformamide (50 ml) was added sodium cyanide (620 mg) at room temperature, and the mixture was stirred at the same temperature for 3 hours. Then, to the mixture was added dropwise a solution of ethyl acrylate (5.2 ml) in N,N-dimethylformamide (25 ml), and the resulting mixture was stirred at the room temperature for 3 hours. The reaction mixture was poured into water and extracted with diethyl ether. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. The resulting residue was purified by silica gel column chromatography (solvent: hexane:ethyl acetate=20:1) to obtain ethyl 4-(4-chloro-3-fluorophenyl)-4-oxobutyrate (9.4 g) as pale yellowish powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759373B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-1bff6aff966f41ff8e7087dd95c4d335 |
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| Source note | uspto-grants-2010_07 |
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