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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444970Generated: November 1, 2026

Hydrochloric Acid → Ethyl 3-(4-methylphenyl)-3-oxopropanoate

https://huagongshe.com/reaction/1444970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-TolunitrileHCID 7724—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178472539HCID 178472539—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(4-methylphenyl)-3-oxopropanoateHCID 29263791%

Reaction Steps

Under nitrogen atmosphere, 30 mL of THF was added to 6.09 g (10 mmol, 1.0 equivlanet) of (BrZnCH2COOEt.THF)2. Under argon atmosphere, a solution of 1.17 g (10 mmol) of p-tolunitrile in 5 mL of THF was added dropwise while stirring at 0˜5° C. The mixture was stirred 20˜25° C. for 46 hours. 15 mL of 10% hydrochloric acid was 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 1.88 g of the desired product (yield 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662974B2
Source datasetuspto-grants-2010_02
ORD IDord-65865b532d6144f7b880709855ffc1e7
Source noteuspto-grants-2010_02