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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420243Generated: October 25, 2026

Hydrochloric Acid → Ethyl 3-(2-fluorophenyl)-3-oxopropanoate

https://huagongshe.com/reaction/420243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant2-FluorobenzonitrileHCID 67855—
ReactantHCID 178472539HCID 178472539—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(2-fluorophenyl)-3-oxopropanoateHCID 29634292%

Reaction Steps

Under nitrogen atmosphere, 30 mL of THF was added to 6.09 g (10 mmol, 1.0 equivalent) of (BrZnCH2COOEt.THF)2. Under argon atmosphere, a solution of 1.21 g (10 mmol) of 2-fluorobenzonitrile in 5 mL of THF was added dropwise while stirring at 0˜5° C. The mixture was stirred at 20° C.˜25° C. for 46 hours. 15 mL of 10% hydrochloric acid added dropwise at 20° C. or lower, and the mixture was stirred at 20˜25° C. for 1. hour, followed by dilution with 50 mL of ethyl acetate. Then, the layers were separated. The organic layer was washed successively with 15 mL of 1N hydrochloric acid, 20 mL of an aqueous saturated sodium chloride solution, 20 mL (×2) of an aqueous saturated sodium bicarbonate solution, and 20 mL of an aqueous saturated sodium chloride solution. After washing, the organic layer was dried with anhydrous magnesium sulfate. Concentration under reduced pressure afforded 1.94 g of the desired product (yield 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093403B2
Source datasetuspto-grants-2012_01
ORD IDord-018ab8d4cd3e4e69b9978a44b95e74ef
Source noteuspto-grants-2012_01