HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989796Generated: November 1, 2026
1,2-Dichloroethane → Ethyl 2,4,5-trifluorobenzoylacetate
https://huagongshe.com/reaction/1989796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,4,5-Trifluorobenzonitrile | HCID 593813 | — |
| Reactant | Potassium ethylmalonate | HCID 86617294 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | Ethyl 2,4,5-trifluorobenzoylacetate | HCID 2758933 | 80% |
Reaction Steps
To 10 □ of 1,2-dichloroethane were added 1.0 g of 2,4,5-trifluorobenzonitrile, 0.43 g of zinc chloride, and 1.3 g of potassium ethylmalonate, and then the mixture was stirred at reflux. After the reaction was completed, 11 □ of 6 N hydrochloric acid was added to the mixture, which then was stirred at reflux at 90° C. for 1 hour. After confirming completion of the reaction by TLC, the solution was cooled to 20° C., and then an organic layer was separated therefrom. The organic layer was concentrated through distillation under reduced pressure. Thus resulted residue was purified by silica gel column chromatography (eluent: ethylacetate/n-hexane=1/10, v/v) to obtain the title compound in the yield of 80% (1.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642356B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-0a34a13c737c42d29ed0201a6542d316 |
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| Source note | uspto-grants-2010_01 |
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