HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066535Generated: November 2, 2026
Hydrochloric Acid → Ethyl 2-(4-chloro-2-fluorophenyl)-2-formylacetate
https://huagongshe.com/reaction/1066535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-chloro-2-fluorophenylacetate | HCID 4518464 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(4-chloro-2-fluorophenyl)-2-formylacetate | HCID 21200432 | — |
Reaction Steps
Then, 3.6 g of sodium hydride (60% in oil) was suspended in 120 ml of tetrahydrofuran, and the mixture was cooled to 5° C., to which a solution of 17.8 g of ethyl 4-chloro-2-fluorophenylacetate in 120 nm of tetrahydrofliran was slowly added dropwise. The mixture was stirred for 30 minutes with a gradual temperature increase to room temperature, to which 20 ml of ethyl formate was added at room temperature, followed by stirring for 3 hours. Then, the reaction mixture was cooled with ice, to which diluted aqueous hydrochloric acid was added. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried, and concentrated. The residue was subjected to silica gel column chromatography, which afforded 19.1 g of ethyl 2-(4-chloro-2-fluorophenyl)-2-formylacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06242634B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-61ad5ee46d604cefa63f6ffde4ce46bc |
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| Source note | uspto-grants-2001_06 |
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