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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl formateHCID 8025—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-chloro-2-fluorophenylacetateHCID 4518464—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(4-chloro-2-fluorophenyl)-2-formylacetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242634B1
Source datasetuspto-grants-2001_06
ORD IDord-61ad5ee46d604cefa63f6ffde4ce46bc
Source noteuspto-grants-2001_06